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Article

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

BMC medical genomics - 26 Mar 2022

Fu Ying, Huang Shasha, Gao Xue, Han Mingyu, Wang Guojian, Kang Dongyang, Yuan Yongyi, Dai Pu

Abstract excerpt

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 cases with evidenced MYO15A variants from the 2263 Chinese NSHL cases, who underwent next-generation sequencing (NGS), were...

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Identifiers

PMID: 35346193
DOI: 10.1186/s12920-022-01201-3
PMCID: PMC8962197

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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