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- [1] Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese familyINTERNATIONAL JOURNAL OF UROLOGY, 2011, 18 (03) : 240 - 242Li, Jing论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Nephrol, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R ChinaYu, Chaowen论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R ChinaTao, Ye论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Nephrol, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R ChinaYang, Yuan论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R ChinaHu, Zhangxue论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Nephrol, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R ChinaZhang, Sizhong论文数: 0 引用数: 0 h-index: 0机构: Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, Div Human Morbid Genom, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China Sichuan Univ, W China Hosp, Dept Med Genet, Chengdu 610041, Sichuan, Peoples R China
- [2] PKD1 Mutation Is a Biomarker for Autosomal Dominant Polycystic Kidney DiseaseBIOMOLECULES, 2023, 13 (07)Kimura, Tomoki论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanKawano, Haruna论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Adv Informat Genet Dis, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan论文数: 引用数: h-index:机构:Muramoto, Nobuhito论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Tokyo Womens Med Univ, Inst Lab Anim, Human Dis Models, Tokyo 1628666, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanTakano, Toshiaki论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Intractable Dis Res Ctr, Diagnost & Therapeut Intractable Dis, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanLu, Yan论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanEguchi, Hidetaka论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Intractable Dis Res Ctr, Diagnost & Therapeut Intractable Dis, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanWada, Hiroo论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Publ Hlth, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanOkazaki, Yasushi论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Intractable Dis Res Ctr, Diagnost & Therapeut Intractable Dis, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanIde, Hisamitsu论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Digital Therapeut, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, JapanHorie, Shigeo论文数: 0 引用数: 0 h-index: 0机构: Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Adv Informat Genet Dis, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Digital Therapeut, Grad Sch Med, Tokyo 1138431, Japan Juntendo Univ, Dept Urol, Grad Sch Med, Tokyo 1138431, Japan
- [3] Mutational analysis of PKD1 gene in a Chinese family with autosomal dominant polycystic kidney diseaseINTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 8 (10): : 13289 - 13292Liu, Jingyan论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Shandong Prov Hosp, Dept Resp, Jinan 250100, Shandong, Peoples R China Linyi Peoples Hosp, Dept Prehosp Emergency, Linyi 276003, Shandong, Peoples R China Shandong Univ, Shandong Prov Hosp, Dept Resp, Jinan 250100, Shandong, Peoples R ChinaLi, Lanrong论文数: 0 引用数: 0 h-index: 0机构: Linyi Peoples Hosp, Dept Prehosp Emergency, Linyi 276003, Shandong, Peoples R China Shandong Univ, Shandong Prov Hosp, Dept Resp, Jinan 250100, Shandong, Peoples R ChinaLiu, Qingmin论文数: 0 引用数: 0 h-index: 0机构: Linyi Peoples Hosp, Intens Care Unit, Linyi 276003, Shandong, Peoples R China Shandong Univ, Shandong Prov Hosp, Dept Resp, Jinan 250100, Shandong, Peoples R China
- [4] Mutation analysis of the PKD1 and PKD2 gene in patients with autosomal dominant polycystic kidney disease (ADPKD).KIDNEY INTERNATIONAL, 1999, 55 (04) : 1599 - 1599Kim, UK论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaLee, CC论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaLee, KB论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaKim, DJ论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaOh, MR论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaKim, JS论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaLee, K论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South KoreaJin, DK论文数: 0 引用数: 0 h-index: 0机构: Seoul Natl Univ, Dept Mol Biol, Seoul 151, South Korea
- [5] A de novo PKD1 mutation in a Chinese family with autosomal dominant polycystic kidney diseaseMEDICINE, 2024, 103 (13) : E27853Wei, Ting论文数: 0 引用数: 0 h-index: 0机构: Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaZhang, Bing论文数: 0 引用数: 0 h-index: 0机构: Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaTang, Wei论文数: 0 引用数: 0 h-index: 0机构: Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaLi, Xin论文数: 0 引用数: 0 h-index: 0机构: Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaShuai, Zhuang论文数: 0 引用数: 0 h-index: 0机构: North Sichuan Med Coll, Affiliated Hosp, Dept Cardiol Med, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaTang, Tao论文数: 0 引用数: 0 h-index: 0机构: North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaZhang, Yueyang论文数: 0 引用数: 0 h-index: 0机构: North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaDeng, Lin论文数: 0 引用数: 0 h-index: 0机构: North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R ChinaLiu, Qingsong论文数: 0 引用数: 0 h-index: 0机构: Univ Elect Sci & Technol China, Chengdu Womens & Childrens Cent Hosp, Sch Med, Dept Prenatal Diag, Chengdu, Peoples R China Univ Elect Sci & Technol China, Chengdu Womens & Childrens Cent Hosp, Sch Med, Dept Prenatal Diag, Chengdu 610000, Peoples R China Nanchong Cent Hosp, Clin Med Coll 2, North Sichuan Med Coll, Dept Med Lab, Nanchong, Peoples R China
- [6] Autosomal dominant polycystic kidney disease: detection of a novel mutation in the PKD1 gene.MEDICINA-BUENOS AIRES, 1999, 59 (02) : 133 - 137Iglesias, DM论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaManrique, M论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaArrizurieta, EE论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaKornblihtt, AR论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaHerrera, M论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaMartin, RS论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, ArgentinaBernath, VA论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Med Alfredo Lanari, Fac Med, RA-1427 Buenos Aires, DF, Argentina
- [7] A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney DiseaseINTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, 2016, 5 (02) : 123 - +Jamshidi, Javad论文数: 0 引用数: 0 h-index: 0机构: Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, IranNaderi, Hamed论文数: 0 引用数: 0 h-index: 0机构: Univ Tehran Med Sci, Imam Khomeini Hosp, Sch Med, Dept Neurol, Tehran, Iran Univ Tehran Med Sci, Iranian Ctr Neurol Res, Tehran, Iran Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, IranTaghavi, Shaghayegh论文数: 0 引用数: 0 h-index: 0机构: Shahid Beheshti Univ Med Sci, Sch Med, Dept Med Genet, Tehran, Iran Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [8] Novel method for the genomic analysis of PKD1 mutation in autosomal dominant polycystic kidney diseaseFRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2023, 10Shang, Shunlai论文数: 0 引用数: 0 h-index: 0机构: China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R China Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China Nankai Univ, Sch Med, Tianjin, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaWang, Chao论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China Guangdong Pharmaceut Univ, Clin Med Sch, Guangzhou, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaChen, Lang论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaShen, Wanjun论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaXie, Yuansheng论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaLi, Wenge论文数: 0 引用数: 0 h-index: 0机构: China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R ChinaLi, Qinggang论文数: 0 引用数: 0 h-index: 0机构: Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis, Med Sch Chinese PLA,Dept Nephrol, Beijing, Peoples R China China Japan Friendship Hosp, Dept Nephrol, Beijing, Peoples R China
- [9] Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney DiseaseJOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2016, 27 (03): : 722 - 729Audrezet, Marie-Pierre论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceCorbiere, Christine论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceLebbah, Said论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceMoriniere, Vincent论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceBroux, Francoise论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Charles Nicolle, Pediat Nephrol & Hemodialysis Unit, Dept Med Pediat, Rouen, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceLouillet, Ferielle论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Charles Nicolle, Pediat Nephrol & Hemodialysis Unit, Dept Med Pediat, Rouen, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceFischbach, Michel论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Strasbourg Strasbourg, Dept Pediat 1, Strasbourg, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceZaloszyc, Ariane论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Strasbourg Strasbourg, Dept Pediat 1, Strasbourg, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceCloarec, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Tours, Clocheville Hosp, Dept Pediat Nephrol & Hemodialysis, Tours, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceMerieau, Elodie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Tours, Clocheville Hosp, Dept Pediat Nephrol & Hemodialysis, Tours, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceBaudouin, Veronique论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Robert Debre, AP HP, Dept Pediat Nephrol, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceDeschenes, Georges论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Robert Debre, AP HP, Dept Pediat Nephrol, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceRoussey, Gwenaelle论文数: 0 引用数: 0 h-index: 0机构: Nantes Univ Hosp, Dept Pediat, Nantes, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceMaestri, Sandrine论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceVisconti, Chiara论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceBoyer, Olivia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Paris 05, Sorbonne Paris Cite, INSERM, U1163,Lab Hereditary Kidney Dis, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceAbel, Carine论文数: 0 引用数: 0 h-index: 0机构: Croix Rousse Hosp Lyon, Hosp Civils Lyon, Dept Med Genet, Lyon, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceLahoche, Annie论文数: 0 引用数: 0 h-index: 0机构: Reg Univ Hosp Lille, Jeanne Flandre Hosp, Pediat Nephrol Unit, Lille, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceRandrianaivo, Hanitra论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp St Pierre Reunion, Med Genet Unit, St Pierre, Reunion, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceBesenay, Lucie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Estaing, Dept Pediat & Pediat Nephrol, Clermont Ferrand, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceMekahli, Djalila论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Leuven, Dept Pediat Nephrol, Leuven, Belgium Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceOuertani, Ines论文数: 0 引用数: 0 h-index: 0机构: Charles Nicolle Hosp, Dept Congenital & Inherited Dis, Tunis, Tunisia Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceDecramer, Stephane论文数: 0 引用数: 0 h-index: 0机构: Children Hosp Toulouse, Dept Pediat Nephrol, Toulouse, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceRyckenwaert, Amelie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Dept Pediat, Rennes, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceCornec-Le Gall, Emilie论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceSalomon, Remi论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Paris 05, Sorbonne Paris Cite, INSERM, U1163,Lab Hereditary Kidney Dis, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceFerec, Claude论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, FranceHeidet, Laurence论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Necker Enfants Malades Paris, AP HP, Dept Pediat Nephrol, Ctr Reference Malad Renales Hereditaires Enfant &, Paris, France Univ Hosp Brest, Inst Natl Sante & Rech Med, Lab Mol Genet & Histocompatibil, U1078, Brest, France
- [10] Ace gene polymorphism in patients with PKD1 autosomal dominant polycystic kidney disease (PKD1 ADPKD)JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1996, 7 (09): : A1807 - A1807Baboolal, K论文数: 0 引用数: 0 h-index: 0机构: CARDIFF ROYAL INFIRM, INST NEPHROL, CARDIFF CF2 1SZ, S GLAM, WALESDaniels, J论文数: 0 引用数: 0 h-index: 0机构: CARDIFF ROYAL INFIRM, INST NEPHROL, CARDIFF CF2 1SZ, S GLAM, WALESRavine, D论文数: 0 引用数: 0 h-index: 0机构: CARDIFF ROYAL INFIRM, INST NEPHROL, CARDIFF CF2 1SZ, S GLAM, WALESColes, GA论文数: 0 引用数: 0 h-index: 0机构: CARDIFF ROYAL INFIRM, INST NEPHROL, CARDIFF CF2 1SZ, S GLAM, WALESWilliams, JD论文数: 0 引用数: 0 h-index: 0机构: CARDIFF ROYAL INFIRM, INST NEPHROL, CARDIFF CF2 1SZ, S GLAM, WALES