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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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| Gepubliceerd in: | Hum Genome Var |
|---|---|
| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group UK
2018
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| Onderwerpen: | |
| Online toegang: | 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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