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Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran
BACKGROUND: The common GJB2 gene mutation (35delG) has been previously reported from Iranian patients that were affected with nonsyndromic autosomal recessive deafness. We, therefore, for the first time, investigated the prevalence and frequency of the GJB2 gene mutation in the Iranian deaf populati...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2846572/ https://ncbi.nlm.nih.gov/pubmed/20407643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.50863 |
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