Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

Abstract 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 possibl...

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主要な著者: Yingjie Zhou (著者), Muhammad Tariq (著者), Sijie He (著者), Uzma Abdullah (著者), Jianguo Zhang (著者), Shahid Mahmood Baig (著者)
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出版事項: BMC, 2020-07-01T00:00:00Z.
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