Identification of a novel mutation in CRYM in a Chinese family with hearing loss using whole-exome sequencing

Previous studies have identified ~50 genes that contribute to non-syndromic autosomal dominant sensorineural deafness (DFNA). However, in numerous families with hearing loss, the specific gene mutation remains to be identified. In the present study, the clinical characteristics and gene mutations we...

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Detalles Bibliográficos
Autores principales: Wang, Min, Li, Qian, Deng, Anchun, Zhu, Xianbai, Yang, Junjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388290/
https://www.ncbi.nlm.nih.gov/pubmed/32742378
http://dx.doi.org/10.3892/etm.2020.8890

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388290/
https://www.ncbi.nlm.nih.gov/pubmed/32742378
http://dx.doi.org/10.3892/etm.2020.8890

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