Loading...
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...
Na minha lista:
| Udgivet i: | Hum Genome Var |
|---|---|
| Main Authors: | , , , |
| 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|