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Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
BACKGROUND: Hearing loss is the most common sensory defect, and it affects over 6% of the population worldwide. Approximately 50–60% of hearing loss patients are attributed to genetic causes. Currently, more than 100 genes have been reported to cause non-syndromic hearing loss. It is possible and ef...
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| Publié dans: | BMC Med Genet |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7368710/ https://ncbi.nlm.nih.gov/pubmed/32682410 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01087-x |
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