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Identification of four TMC1 variations in different Chinese families with hereditary hearing loss

BACKGROUND: Variants in TMC1 (transmembrane channel‐like 1) can cause both autosomal dominant and recessive hearing loss in human population. Mice with Tmc1 variants have been shown to be ideal animal models for gene therapy. In this article, we report four TMC1 variants in four different Chinese fa...

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Publicat a:Mol Genet Genomic Med
Autors principals: Wang, Hongyang, Wu, Kaiwen, Guan, Jing, Yang, Ju, Xie, Linyi, Xiong, Fen, Lan, Lan, Wang, Dayong, Wang, Qiuju
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6081220/
https://ncbi.nlm.nih.gov/pubmed/29654653
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.394
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