Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness

BACKGROUND: Nonsyndromic hearing loss is clinically and genetically heterogeneous. In this study, we characterized the clinical features of 12 Chinese Han deaf families in which mutations in common deafness genes GJB2, SLC26A4, and MT‐RNR1 were excluded. METHODS: Targeted next‐generation sequencing...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: Wu, Di, Huang, Weiyuan, Xu, Zhenhang, Li, Shuo, Zhang, Jie, Chen, Xiaohua, Tang, Yan, Qiu, Jinhong, Wang, Zhixia, Duan, Xuchu, Zhang, Luping
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Clinical Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7196461/
https://ncbi.nlm.nih.gov/pubmed/32048449
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1177
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados