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Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation
BACKGROUND: Genetic factors play an important role in hearing loss, contributing to approximately 60 % of cases of congenital hearing loss. Autosomal dominant deafness accounts for approximately 20 % of cases of hereditary hearing loss. Diseases with autosomal dominant inheritance often show pleiotr...
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| Publicado no: | BMC Genet |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4736096/ https://ncbi.nlm.nih.gov/pubmed/26832775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-016-0333-1 |
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