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Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort
BACKGROUND: Hearing loss or hearing impairment is a clinically and genetically heterogeneous disorder. More than 117 genes were discovered to date in hereditary, nonsyndromic hearing loss (NSHL). Identifying novel gene variants and their frequency in specific populations is valuable for public healt...
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| Vydáno v: | Mol Genet Genomic Med |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6732339/ https://ncbi.nlm.nih.gov/pubmed/31389194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.917 |
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