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- [31] Distinct neurodevelopmental and epileptic phenotypes associated with gain- and loss-of-function GABRB2 variantsEBIOMEDICINE, 2024, 106Mohammadi, Nazanin Azarinejad论文数: 0 引用数: 0 h-index: 0机构: Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkAhring, Philip Kiaer论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Med Sci, Sydney, NSW 2006, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLiao, Vivian Wan Yu论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Med Sci, Sydney, NSW 2006, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkChua, Han Chow论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Charles Perkins Ctr, Sydney Pharm Sch, Sydney, NSW 2006, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkRosa, Sebastian Ortiz de la论文数: 0 引用数: 0 h-index: 0机构: Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkJohannesen, Katrine Marie论文数: 0 引用数: 0 h-index: 0机构: Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Hosp Copenhagen, Dept Genet, Rigshospitalet, Copenhagen, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMichaeli-Yossef, Yael论文数: 0 引用数: 0 h-index: 0机构: Wolfson Med Ctr, Pediat Neurol Unit, Holon, Israel Wolfson Med Ctr, Metab Neurogenet Clin, Holon, Israel Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkVincent-Devulder, Aline论文数: 0 引用数: 0 h-index: 0机构: CHU Cote Nacre, Genet Dept, Caen, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMeridda, Catherine论文数: 0 引用数: 0 h-index: 0机构: CHU Cote Nacre, Genet Dept, Caen, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBruel, Ange-Line论文数: 0 引用数: 0 h-index: 0机构: CHU Cote Nacre, Genet Dept, Caen, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark论文数: 引用数: h-index:机构:Patel, Chirag论文数: 0 引用数: 0 h-index: 0机构: Royal Brisbane & Womens Hosp, Genet Hlth Queensland, Brisbane, Qld 4029, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkKlepper, Joerg论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Aschaffenburg Alzenau, Aschaffenburg, Germany Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBonanni, Paolo论文数: 0 引用数: 0 h-index: 0机构: IRCCS E Medea Sci Inst, Epilepsy Unit, Conegliano, Treviso, Italy Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMinghetti, Sara论文数: 0 引用数: 0 h-index: 0机构: IRCCS E Medea Sci Inst, Clin Neurophysiol Unit, Bosisio Parini, Italy Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkTrivisano, Marina论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, IRCCS, European Reference NetworkEpiCARE, Neurol Epilepsy & Movement Disorders, Rome, Italy Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkSpecchio, Nicola论文数: 0 引用数: 0 h-index: 0机构: Bambino Gesu Pediat Hosp, IRCCS, European Reference NetworkEpiCARE, Neurol Epilepsy & Movement Disorders, Rome, Italy Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkAmor, David论文数: 0 引用数: 0 h-index: 0机构: Murdoch Childrens Res Inst, Melbourne, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkAuvin, Stephane论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Child Neurol & Epilepsy, Paris, France Robert Debre Hosp, Ctr Rare Epilepsies Pediat Neurol, Paris, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkBaer, Sarah论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, French Reference Ctr Rare Epilepsies CREER, Dept Paediat Neurol, Strasbourg, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMeyer, Pierre论文数: 0 引用数: 0 h-index: 0机构: Montpellier Univ, Univ Hosp Montpellier, Paediat Neurol Dept, Phymedexp,Inserm,CNRS, Montpellier, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMilh, Mathieu论文数: 0 引用数: 0 h-index: 0机构: Timone Childrens Hosp, AP HM, Dept Pediat Neurol, Marseille, France Aix Marseille Univ, Fac Med Timone, INSERM, MMG,U1251,ERN EpiCARE, Marseille, France Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkSalpietro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy IRCCS Giannina Gaslini Inst, Pediat Neurol & Muscular Dis Unit, Genoa, Italy Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMaroo, Reza论文数: 0 引用数: 0 h-index: 0机构: UCL Queen Sq Inst Neurol, Dept Neuromusc Disorders, London, England Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkLemke, Johannes R.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Univ Leipzig, Ctr Rare Dis, Med Ctr, Leipzig, Germany Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkWeckhuysen, Sarah论文数: 0 引用数: 0 h-index: 0机构: VIB, VIB Ctr Mol Neurol, Appl & Translat Neurogenom Grp, Antwerp, Belgium Antwerp Univ Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, Fac Med & Hlth Sci, Translat Neurosci, Antwerp, Belgium Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkChristophersen, Palle论文数: 0 引用数: 0 h-index: 0机构: Saniona AS, Ballerup, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkRubboli, Guido论文数: 0 引用数: 0 h-index: 0机构: Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkChebib, Mary论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Med Sci, Sydney, NSW 2006, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkJensen, Anders A.论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Fac Hlth & Med Sci, Dept Drug Design & Pharmacol, Copenhagen, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkAbsalom, Nathan L.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Med Sci, Sydney, NSW 2006, Australia Western Sydney Univ, Sch Sci, Sydney, NSW 2751, Australia Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, DenmarkMoller, Rikke Steensbjerre论文数: 0 引用数: 0 h-index: 0机构: Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Filadelfia ERN EpiCARE, Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark
- [32] The chromosome 5 GABA A receptor genes GABRA1 and GABRB2 confer risk of schizophrenia and are correlated with altered GABA pathway transcript levelsAMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 18 - 18Petryshen, TL论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAKirby, AN论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAPato, CN论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USATahl, AR论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAMiddleton, FA论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USARockwell, G论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USASchwab, SG论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAWildenauer, DB论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAAldinger, KA论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAWaggoner, SG论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAMorley, CP论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAMcGann, L论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAGentile, KL论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAMedeiros, H论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAAzevedo, MH论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USADaly, MJ论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USAPato, MT论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USASklar, P论文数: 0 引用数: 0 h-index: 0机构: MIT, Broad Inst, Cambridge, MA 02139 USA
- [33] Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): A cohort study, review of literature, and genotype-phenotype correlationEPILEPSIA, 2022, 63 (10) : 2519 - 2533Maillard, Pierre-Yves论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceBaer, Sarah论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Univ Strasbourg, Inst Genet & Mol & Cellular Biol IGBMC, CNRS, UMR7104,INSERM,U1258, Illkirch Graffenstaden, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceSchaefer, Elise论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceDesnous, Beatrice论文数: 0 引用数: 0 h-index: 0机构: La Timone Childrens Hosp, AP HM, Dept Pediat Neurol, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceVilleneuve, Nathalie论文数: 0 引用数: 0 h-index: 0机构: La Timone Childrens Hosp, AP HM, Dept Pediat Neurol, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceLepine, Anne论文数: 0 引用数: 0 h-index: 0机构: La Timone Childrens Hosp, AP HM, Dept Pediat Neurol, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceFabre, Alexandre论文数: 0 引用数: 0 h-index: 0机构: Timone Enfant, AP HM, Pediat Multidisciplinary Unit, Marseille, France Aix Marseille Univ, INSERM, GMGF, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceLacoste, Caroline论文数: 0 引用数: 0 h-index: 0机构: La Timone Childrens Hosp, Dept Med Genet, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceEl Chehadeh, Salima论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, France Univ Strasbourg, Inst Genet & Mol & Cellular Biol IGBMC, CNRS, UMR7104,INSERM,U1258, Illkirch Graffenstaden, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePiton, Amelie论文数: 0 引用数: 0 h-index: 0机构: Univ Strasbourg, Inst Genet & Mol & Cellular Biol IGBMC, CNRS, UMR7104,INSERM,U1258, Illkirch Graffenstaden, France Hop Univ Strasbourg, Inst Genet Med Alsace, Lab Genet Diag, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePorter, Louise Frances论文数: 0 引用数: 0 h-index: 0机构: Inst Genet Med Alsace, Ctr Reference Affect Rares Genet Ophtalmol CARGO, Dept Med Genet, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePerriard, Caroline论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceWarde, Marie-Therese Abi论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceSpitz, Marie-Aude论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceLaugel, Vincent论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceLesca, Gaetan论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Dept Genet, Bron, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePutoux, Audrey论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Dept Genet, Bron, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceVille, Dorothee论文数: 0 引用数: 0 h-index: 0机构: Lyon Univ Hosp, Mother Child Womens Hosp, Pediat Neurol Dept, Lyon, France Lyon Univ Hosp, Mother Child Womens Hosp, Reference Ctr Rare Epilepsies, Lyon, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceMignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, Dept Genet, Paris, France Sorbonne Univ, Hop Armand Trousseau, AP HP, Paris, France Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceHeron, Delphine论文数: 0 引用数: 0 h-index: 0机构: Sorbonne Univ, Grp Hosp Pitie Salpetriere, Dept Genet, Paris, France Sorbonne Univ, Hop Armand Trousseau, AP HP, Paris, France Ctr Reference Deficiences Intellectuelles Causes, Paris, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceNabbout, Rima论文数: 0 引用数: 0 h-index: 0机构: Univ Paris, Necker Enfants Malades Univ Hosp, AP HP, Dept Pediat Neurol,Reference Ctr Rare Epilepsies, Paris, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Roubertie, Agathe论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, CHU Montpellier, INSERM, Pediat Neurol Dept,INM, Montpellier, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceMeyer, Pierre论文数: 0 引用数: 0 h-index: 0机构: Univ Montpellier, CHU Montpellier, INSERM, Pediat Neurol Dept,INM, Montpellier, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePaquis-Flucklinger, Veronique论文数: 0 引用数: 0 h-index: 0机构: Nice Univ Hosp, Dept Med Genet, Nice, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FrancePatat, Olivier论文数: 0 引用数: 0 h-index: 0机构: CHU Toulouse Purpan, Dept Med Genet, Toulouse, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceLefranc, Jeremie论文数: 0 引用数: 0 h-index: 0机构: CHU Brest, Pediat Dept, Brest, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceGerard, Marion论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ Caen, Dept Med Genet, Caen, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, Francede Bellescize, Julietta论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Lyon HCL, Reference Ctr Rare Epilepsies, Paediat Clin Epileptol & Funct Neurol Dept, ERN EpiCARE, Lyon, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceVillard, Laurent论文数: 0 引用数: 0 h-index: 0机构: Timone Enfant, AP HM, Pediat Multidisciplinary Unit, Marseille, France Aix Marseille Univ, Fac Medecine Timone, MMG, INSERM,U1251,ERN Epicare, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceDe Saint Martin, Anne论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Dept Neuropediat, ERN EpiCare, Strasbourg, France Univ Strasbourg, Inst Genet & Mol & Cellular Biol IGBMC, CNRS, UMR7104,INSERM,U1258, Illkirch Graffenstaden, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, FranceMilh, Mathieu论文数: 0 引用数: 0 h-index: 0机构: Aix Marseille Univ, Fac Medecine Timone, MMG, INSERM,U1251,ERN Epicare, Marseille, France Hop Univ Strasbourg, Dept Med Genet, IGMA, Strasbourg, France
- [34] Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizuresNEUROSCIENCE LETTERS, 2005, 383 (03) : 220 - 224Ito, M论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Child Neurol, Okayama 7008558, JapanOhmori, I论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Child Neurol, Okayama 7008558, JapanNakahori, T论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Child Neurol, Okayama 7008558, JapanOuchida, M论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Child Neurol, Okayama 7008558, JapanOhtsuka, Y论文数: 0 引用数: 0 h-index: 0机构: Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Child Neurol, Okayama 7008558, Japan
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