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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Udgivet i:BMC Med Genet
Main Authors: Zhou, Yingjie, Tariq, Muhammad, He, Sijie, Abdullah, Uzma, Zhang, Jianguo, Baig, Shahid Mahmood
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2020
Fag:
Research Article
Online adgang: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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