共 37 条
- [21] Identification of a novel homozygous mutation in the MYO15A gene in a Kazakh family with non-syndromic hearing lossINTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2019, 125 : 128 - 132Zhou, HongbinKuermanhan, AhanZhang, ZhihuaWang, WenjingDong, JieZhou, ZhouMu, JianZhao, LinWang, JianLi, BingChen, Biaobang
- [22] Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patientsBMC MEDICAL GENOMICS, 2022, 15 (01)Fu, YingHuang, ShashaGao, XueHan, MingyuWang, GuojianKang, DongyangYuan, YongyiDai, Pu
- [23] Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeHUMAN GENETICS, 2001, 109 (05) : 535 - 541Liburd, NGhosh, MRiazuddin, SNaz, SKhan, SAhmed, ZRiazuddin, SLiang, YMenon, PSNSmith, TSmith, ACMChen, KSLupski, JRWilcox, ERPotocki, LFriedman, TB
- [24] Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeHuman Genetics, 2001, 109 : 535 - 541Nikki LiburdManju GhoshSaima RiazuddinSadaf NazShaheen KhanZubair AhmedSheikh RiazuddinYong LiangPuthezhath S. MenonTenesha SmithAnn C. SmithKen-Shiung ChenJames R. LupskiEdward R. WilcoxLorraine PotockiThomas B. Friedman
- [25] Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing lossBMC MEDICAL GENETICS, 2019, 20Zhang, JingGuan, JingWang, HongyangYin, LinweiWang, DayongZhao, LidongZhou, HuifangWang, Qiuju
- [26] Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non-syndromic hearing lossJOURNAL OF CLINICAL LABORATORY ANALYSIS, 2022, 36 (10)Wang, LumingZhang, YueXue, QiuxiaHuang, PinghuaLiu, Xiaodan
- [27] Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean familiesBMC MEDICAL GENETICS, 2013, 14Woo, Hae-MiPark, Hong-JoonBaek, Jeong-InPark, Mi-HyunKim, Un-KyungSagong, BorumKoo, Soo Kyung
- [28] Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This LocusGENETIC TESTING AND MOLECULAR BIOMARKERS, 2009, 13 (01) : 147 - 151Belguith, HanenAifa-Hmani, MouniraDhouib, HouriaBen Said, MariemMosrati, Mohamed AliLahmar, ImedMoalla, JihenCharfeddine, IlhemDriss, NabilBen Arab, SaidaGhorbel, AbdelmonemAyadi, HammadiMasmoudi, Saber
- [29] Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing lossMOLECULAR BIOLOGY REPORTS, 2020, 47 (07) : 5355 - 5364Sarmadi, AkramNasrniya, SamaneNarrei, SinaNouri, ZahraAbtahi, HamidrezaTabatabaiefar, Mohammad Amin
- [30] Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing lossMolecular Biology Reports, 2020, 47 : 5355 - 5364Akram SarmadiSamane NasrniyaSina NarreiZahra NouriHamidreza AbtahiMohammad Amin Tabatabaiefar