Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non-syndromic hearing loss

Hearing loss is the most common sensory deficit in humans and gaining a better understanding of the underlying causes is necessary to improve counseling and rehabilitation. In the present study, a genetic analysis of a Chinese family with autosomal dominant non-syndromic progressive hearing impairme...

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Detalles Bibliográficos
Autores principales: TAN, MINXING, SHEN, XIAOFEI, YAO, JUN, WEI, QINJUN, LU, YAJIE, CAO, XIN, XING, GUANGQIAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214331/
https://www.ncbi.nlm.nih.gov/pubmed/25242383
http://dx.doi.org/10.3892/ijmm.2014.1939

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214331/
https://www.ncbi.nlm.nih.gov/pubmed/25242383
http://dx.doi.org/10.3892/ijmm.2014.1939

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