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

• 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)
• フォーマット: 図書
• 出版事項: BMC, 2020-07-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

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...