Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

Congenital deafness is one of the most common causes of disability in humans, and more than half of cases are caused by genetic factors. Mutations of the MYO15A gene are the third most common cause of hereditary hearing loss. Using next-generation sequencing combined with auditory tests, two novel c...

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Detalles Bibliográficos
Autores principales: Wang, Xiao-Hui, Xie, Le, Chen, Sen, Xu, Kai, Bai, Xue, Jin, Yuan, Qiu, Yue, Liu, Xiao-Zhou, Sun, Yu, Kong, Wei-Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140830/
https://www.ncbi.nlm.nih.gov/pubmed/34093702
http://dx.doi.org/10.1155/2021/9957712

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140830/
https://www.ncbi.nlm.nih.gov/pubmed/34093702
http://dx.doi.org/10.1155/2021/9957712

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