Whole-exome sequencing of de novo genetic variants in a Chinese family with a sporadic case of congenital nonsyndromic hearing loss [version 1; peer review: 1 approved, 1 approved with reservations]
Hu, Sijing, Zhang, Hao, Liu, Yunqiang, Liu, Mohan, Li, Jingjing, Liao, Sonia
Published in F1000 research (2021)
Published in F1000 research (2021)
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