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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Detaylı Bibliyografya
Asıl Yazarlar: Godbole, Koumudi, Hemavathi, J., Vaid, Neelam, Pandit, Anand N., Sandeep, M. N., Chandak, G. R.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer-Verlag 2010
Konular:
Original Article
Online Erişim: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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