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Article

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

Journal of translational medicine - 17 Dec 2013

Xin Feng, Yuan Yongyi, Deng Xiaoming, Han Mingyu, Wang Guojian, Zhao Jiandong, Gao Xue, Liu Jun, Yu Fei, Han Dongyi, Dai Pu

Abstract excerpt

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 counseling to these families, we investigated the molecular etiology of nonsyndromic deafness in this population....

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Identifiers

PMID: 24341454
DOI: 10.1186/1479-5876-11-312
PMCID: PMC3878508

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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