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

• Egile Nagusiak: Kaifeng Zheng (Egilea), Sheng Lin (Egilea), Jian Gao (Egilea), Shiguo Chen (Egilea), Jindi Su (Egilea), Zhiqiang Liu (Egilea), Shan Duan (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2024-01-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: 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...