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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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Publicado en:Hum Genome Var
Main Authors: Abe, Satoko, Takeda, Hidehiko, Nishio, Shin-ya, Usami, Shin-ichi
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group UK 2018
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6105593/
https://ncbi.nlm.nih.gov/pubmed/30155266
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-018-0023-9
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