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A systematic review and meta-analysis of 235delC mutation of GJB2 gene
BACKGROUND: The 235delC mutation of GJB2 gene is considered as a risk factor for the non-syndromic hearing loss (NSHL), and a significant difference in the frequency and distribution of the 235delC mutation has been described world widely. METHODS: A systematic review was performed by means of a met...
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| Główni autorzy: | , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
BioMed Central
2012
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3443034/ https://ncbi.nlm.nih.gov/pubmed/22747691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-10-136 |
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