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Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations
Mutations in the GJB2 gene are the most common cause of pre-lingual hearing loss (HL) worldwide. Previous studies have shown the frequency of GJB2 mutations to be 16% in Iran, but varies among different ethnic groups. Here, we have reviewed results from previous published mutation reports to provide...
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| Yayımlandı: | Intractable Rare Dis Res |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6743427/ https://ncbi.nlm.nih.gov/pubmed/31523594 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2019.01070 |
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