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

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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Bibliographic Details
Main Authors: Ying Fu, Shasha Huang, Xue Gao, Mingyu Han, Guojian Wang, Dongyang Kang, Yongyi Yuan, Pu Dai
Format: Article
Language:English
Published: BMC 2022-03-01
Series:BMC Medical Genomics
Subjects:
MYO15A
DFNB3
Hearing loss (HL)
Non-syndromic sensorineural hearing loss (NSHL)
Online Access:https://doi.org/10.1186/s12920-022-01201-3

Internet

https://doi.org/10.1186/s12920-022-01201-3

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