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Contribution of GJB2 mutations to hearing loss in the Hazara Division of Pakistan
Mutations of GJB2, which encodes connexin 26, are the most common cause of hereditary hearing loss in many human populations. This study was initiated to determine the prevalence of GJB2 mutations in individuals with hearing loss from the Hazara Division in Pakistan. We recruited 70 participants wit...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3708968/ https://ncbi.nlm.nih.gov/pubmed/23504403 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10528-013-9583-z |
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