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Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing loss and absence of other clinical manifestations. The aim of this study is to identify the pathogenic gene in a four-generation consanguineous C...

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Bibliografski detalji
Izdano u:PLoS One
Glavni autori: Xia, Hong, Huang, Xiangjun, Guo, Yi, Hu, Pengzhi, He, Guangxiang, Deng, Xiong, Xu, Hongbo, Yang, Zhijian, Deng, Hao
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2015
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4550393/
https://ncbi.nlm.nih.gov/pubmed/26308726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0136306
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