Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

BACKGROUND: Each year in China, 30,000 babies are born with congenital hearing impairment. However, the molecular etiology of hearing impairment in the Yunnan Province population where more than 52 minorities live has not been thoroughly investigated. To provide appropriate genetic testing and couns...

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Detalhes bibliográficos
Main Authors: Xin, Feng, Yuan, Yongyi, Deng, Xiaoming, Han, Mingyu, Wang, Guojian, Zhao, Jiandong, Gao, Xue, Liu, Jun, Yu, Fei, Han, Dongyi, Dai, Pu
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3878508/
https://ncbi.nlm.nih.gov/pubmed/24341454
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-11-312
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