Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families
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 gene...
Source: BMC Medical Genetics - Category: Genetics & Stem Cells Authors: Yingjie Zhou, Muhammad Tariq, Sijie He, Uzma Abdullah, Jianguo Zhang and Shahid Mahmood Baig Tags: Research article Source Type: research
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