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

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

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...

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Main Authors: Kaifeng Zheng (Author), Sheng Lin (Author), Jian Gao (Author), Shiguo Chen (Author), Jindi Su (Author), Zhiqiang Liu (Author), Shan Duan (Author)
Format: Book
Published: BMC, 2024-01-01T00:00:00Z.
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