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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Hongyang, Wu, Kaiwen, Guan, Jing, Yang, Ju, Xie, Linyi, Xiong, Fen, Lan, Lan, Wang, Dayong, Wang, Qiuju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081220/
https://www.ncbi.nlm.nih.gov/pubmed/29654653
http://dx.doi.org/10.1002/mgg3.394

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081220/
https://www.ncbi.nlm.nih.gov/pubmed/29654653
http://dx.doi.org/10.1002/mgg3.394

Ejemplares similares