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Low prevalence of GJB2 mutations in non-syndromic hearing loss in Western India
OBJECTIVES: To identify the prevalence of GJB2 (Cx 26)and GJB6 (Cx 30) mutations in hearing impaired individuals from Western and South India. STUDY DESIGN: Cross-sectional study. METHODS: Families with hearing impaired individuals (prelingual, non-syndromic, sensori-neural hearing loss) were enroll...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3450147/ https://ncbi.nlm.nih.gov/pubmed/23120683 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12070-010-0009-5 |
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