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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...
Guardado en:
| Publicado en: | Mol Genet Genomic Med |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | 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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