Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

Hearing loss is a highly heterogeneous disorder, with more than 60% of congenital cases caused by genetic factors. This study is aimed at identifying the genetic cause of congenital hearing loss in a Chinese Han family. Auditory evaluation before and after cochlear implantation and targeted next-gen...

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Detalles Bibliográficos
Autores principales: Wang, Longhao, Zhao, Lin, Peng, Hu, Xu, Jun, Lin, Yun, Yang, Tao, Wu, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313121/
https://www.ncbi.nlm.nih.gov/pubmed/32617096
http://dx.doi.org/10.1155/2020/6350479

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313121/
https://www.ncbi.nlm.nih.gov/pubmed/32617096
http://dx.doi.org/10.1155/2020/6350479

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