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The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations
Deafness encompasses a series of etiologically heterogeneous disorders with mutations in more than 400 independent genes. However, several studies indicate that a large proportion of both syndromic and nonsyndromic forms of deafness in the racially diverse Indian and Pakistani populations are caused...
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| Publicado no: | Genet Test Mol Biomarkers |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Mary Ann Liebert, Inc.
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4575533/ https://ncbi.nlm.nih.gov/pubmed/26186295 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2015.0023 |
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