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Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

Abstract Background Mutations in the MYO15A gene are a widely recognized cause of autosomal recessive non-syndromic sensorineural hearing loss (NSHL) globally. Here, we examined the role and the genotype-phenotype correlation of MYO15A variants in a cohort of Chinese NSHL cases. Methods Eighty-one c...

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Main Authors: Ying Fu (Author), Shasha Huang (Author), Xue Gao (Author), Mingyu Han (Author), Guojian Wang (Author), Dongyang Kang (Author), Yongyi Yuan (Author), Pu Dai (Author)
Format: Book
Published: BMC, 2022-03-01T00:00:00Z.
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