Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss

• Príomhchruthaitheoirí: Kaifeng Zheng (Údar), Sheng Lin (Údar), Jian Gao (Údar), Shiguo Chen (Údar), Jindi Su (Údar), Zhiqiang Liu (Údar), Shan Duan (Údar)
• Formáid: LEABHAR
• Foilsithe / Cruthaithe: BMC, 2024-01-01T00:00:00Z.
• Ábhair: article
• Rochtain ar líne: Connect to this object online.

Abstract Background Hereditary hearing loss is a highly heterogeneous disorder. This study aimed to identify the genetic cause of a Chinese family with autosomal recessive non-syndromic sensorineural hearing loss (ARNSHL). Methods Clinical information and peripheral blood samples were collected from...