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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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Bibliografiske detaljer
Udgivet i:Hum Genome Var
Main Authors: Abe, Satoko, Takeda, Hidehiko, Nishio, Shin-ya, Usami, Shin-ichi
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group UK 2018
Fag:
Online adgang: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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