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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Detalles Bibliográficos
Autores principales: Xia, Hong, Huang, Xiangjun, Guo, Yi, Hu, Pengzhi, He, Guangxiang, Deng, Xiong, Xu, Hongbo, Yang, Zhijian, Deng, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550393/
https://www.ncbi.nlm.nih.gov/pubmed/26308726
http://dx.doi.org/10.1371/journal.pone.0136306

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550393/
https://www.ncbi.nlm.nih.gov/pubmed/26308726
http://dx.doi.org/10.1371/journal.pone.0136306

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