Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Hearing impairment is one of the most common sensory disease, of which more than 50% is attributed to a genetic etiology. The goal of this research is to explore the genetic cause of a Chinese deafness pedigree who was excluded of GJB2, SLC26A4, or MtDNA12SrRNA variants. Three variants, c.3971C>A...

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Detalles Bibliográficos
Autores principales: Zhang, Fengguo, Xu, Lei, Xiao, Yun, Li, Jianfeng, Bai, Xiaohui, Wang, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907479/
https://www.ncbi.nlm.nih.gov/pubmed/29849560
http://dx.doi.org/10.1155/2018/5898025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5907479/
https://www.ncbi.nlm.nih.gov/pubmed/29849560
http://dx.doi.org/10.1155/2018/5898025

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