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...

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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2020
Fag:
Clinical Report
Online adgang: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
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