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Article

A reverse dot blot assay for the screening of twenty mutations in four genes associated with NSHL in a Chinese population.

PloS one - 1 Jan 2017

Li Siping, Peng Qi, Liao Shengyun, Li Wenrui, Ma Qiang, Lu Xiaomei

Abstract excerpt

BACKGROUND: Congenital deafness is one of the most distressing disorders affecting humanity and exhibits a high incidence worldwide. Most cases of congenital deafness in the Chinese population are caused by defects in a limited number of genes. A convenient and reliable method for detecting common deafness-related gene mutations in the Chinese population is required. METHODS: We developed a PCR-reverse dot blot...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28505178
DOI: 10.1371/journal.pone.0177196
PMCID: PMC5432070

Genes

GJB2
GJB3

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