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Genetics of hearing loss: focus on DFNA2
The purpose of this review is to assess the current literature on deafness nonsyndromic autosomal dominant 2 (DFNA2) hearing loss and the mutations linked to this disorder. Hearing impairment, particularly nonsyndromic hearing loss, affects multiple families across the world. After the identificatio...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3681197/ https://ncbi.nlm.nih.gov/pubmed/23776385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S35525 |
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