A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss

BACKGROUND: MYH14 gene mutations have been suggested to be associated with nonsyndromic/syndromic sensorineural hearing loss. It has been reported that mutations in MYH14 can result in autosomal dominant nonsyndromic deafness-4A (DFNA4). METHODS: In this study, we examined a four-generation Han Chin...

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Detalles Bibliográficos
Autores principales: Wang, Mingming, Zhou, Yicui, Zhang, Fengguo, Fan, Zhaomin, Bai, Xiaohui, Wang, Haibo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382048/
https://www.ncbi.nlm.nih.gov/pubmed/32711451
http://dx.doi.org/10.1186/s12881-020-01086-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382048/
https://www.ncbi.nlm.nih.gov/pubmed/32711451
http://dx.doi.org/10.1186/s12881-020-01086-y

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