Molecular diagnose of a large hearing loss population from China by targeted genome sequencing

Hereditary hearing loss is genetically heterogeneous, with diverse clinical manifestations. Here we performed targeted genome sequencing of 227 hearing loss related genes in 1027 patients with bilateral hearing loss and 520 healthy volunteers with normal hearing to comprehensively identify the molec...

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Detalles Bibliográficos
Autores principales: Wu, Jie, Cao, Zongfu, Su, Yu, Wang, Yang, Cai, Ruikun, Chen, Jiyue, Gao, Bo, Han, Mingyu, Li, Xiaohong, Zhang, DeJun, Gao, Xue, Huang, Shasha, Huang, Quanfei, Yuan, Yongyi, Ma, Xu, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592555/
https://www.ncbi.nlm.nih.gov/pubmed/35982127
http://dx.doi.org/10.1038/s10038-022-01066-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592555/
https://www.ncbi.nlm.nih.gov/pubmed/35982127
http://dx.doi.org/10.1038/s10038-022-01066-5

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