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Mutations of KCNQ4 Channels Associated with Nonsyndromic Progressive Sensorineural Hearing Loss
PURPOSE OF THE REVIEW: This article provides an update on the current progress in identification of KCNQ4 mutations responsible for progressive hearing loss in DFNA2. RECENT FINDINGS: The KCNQ4 gene has been identified at DFNA2 locus on the human chromosome 1p34. DFNA2 is a subtype of autosomal domi...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2743278/ https://ncbi.nlm.nih.gov/pubmed/18797286 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOO.0b013e32830f4aa3 |
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