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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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Dettagli Bibliografici
Pubblicato in:Hum Genome Var
Autori principali: Abe, Satoko, Takeda, Hidehiko, Nishio, Shin-ya, Usami, Shin-ichi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2018
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Accesso online: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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