Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants

Variants in MYH14 are reported to cause autosomal dominant nonsyndromic hereditary hearing loss (ADNSHL), with 34 variants reported to cause hearing loss in various ethnic groups. However, the available information on prevalence, as well as with regard to clinical features, remains fragmentary. In t...

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Detalles Bibliográficos
Autores principales: Hiramatsu, Ken, Nishio, Shin-ya, Kitajiri, Shin-ichiro, Kitano, Tomohiro, Moteki, Hideaki, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535940/
https://www.ncbi.nlm.nih.gov/pubmed/34681017
http://dx.doi.org/10.3390/genes12101623

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535940/
https://www.ncbi.nlm.nih.gov/pubmed/34681017
http://dx.doi.org/10.3390/genes12101623

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