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Article

Deafness gene mutations in newborns in Beijing.

Acta oto-laryngologica - 1 Jan 2016

Han Shujing, Yang Xiaojian, Zhou Yi, Hao Jinsheng, Shen Adong, Xu Fang, Chu Ping, Jin Yaqiong, Lu Jie, Guo Yongli, Shi Jin, Liu Haihong, Ni Xin

Abstract excerpt

OBJECTIVE: To determine the incidence of congenital hearing loss (HL) in newborns by the rate of deafness-related genetic mutations. DESIGN: Clinical study of consecutive newborns in Beijing using allele-specific polymerase chain reaction-based universal array. STUDY SAMPLE: This study tested 37 573 newborns within 3 days after birth, including nine sites in four genes: GJB2 (35 del G, 176 del 16, 235 del C, 299...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 26766211
DOI: 10.3109/00016489.2015.1128121

Genes

GJB2
GJB3

Provenance

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