Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation

EYA4 is a member of the vertebrate eya gene family of transcriptional activators and plays several roles in both embryonic and inner ear development. The majority of EYA4 gene mutations are associated with autosomal dominant non-syndromic hearing loss (DFNA10). In addition, some mutations in this ge...

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Detalles Bibliográficos
Autores principales: Abe, Satoko, Takeda, Hidehiko, Nishio, Shin-ya, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105593/
https://www.ncbi.nlm.nih.gov/pubmed/30155266
http://dx.doi.org/10.1038/s41439-018-0023-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105593/
https://www.ncbi.nlm.nih.gov/pubmed/30155266
http://dx.doi.org/10.1038/s41439-018-0023-9

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