Cargando…
Simultaneous multi-gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing-impairment in Northwest China
The present study aimed to investigate the molecular etiology of nonsyndromic hearing impairment (HI) in hearing impaired populations of Hui, Tibetan, and Tu ethnicities in northwest China. A total of 283 unrelated subjects with HI who attended special education schools in northwest China were enrol...
Autores principales: | Duan, Shi-Hong, Ma, Jian-Li, Yang, Xiao-Long, Guo, Yu-Fen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865789/ https://www.ncbi.nlm.nih.gov/pubmed/28901477 http://dx.doi.org/10.3892/mmr.2017.7431 |
Ejemplares similares
-
Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss
por: Han, Rui, et al.
Publicado: (2017) -
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay
por: Zhang, Fengguo, et al.
Publicado: (2016) -
Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China
por: Duan, Shihong, et al.
Publicado: (2021) -
Application of SNPscan in Genetic Screening for Common Hearing Loss Genes
por: Gao, Zixuan, et al.
Publicado: (2016) -
Simultaneous detection of G6PD mutations using SNPscan in a multiethnic minority area of Southwestern China
por: Wei, Huagui, et al.
Publicado: (2023)