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

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 wi...

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Detalles Bibliográficos
Autores principales: Fu, Ying, Huang, Shasha, Gao, Xue, Han, Mingyu, Wang, Guojian, Kang, Dongyang, Yuan, Yongyi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962197/
https://www.ncbi.nlm.nih.gov/pubmed/35346193
http://dx.doi.org/10.1186/s12920-022-01201-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962197/
https://www.ncbi.nlm.nih.gov/pubmed/35346193
http://dx.doi.org/10.1186/s12920-022-01201-3

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