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Article

Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

International journal of pediatric otorhinolaryngology - 1 Sept 2013

Han Bing, Zong Liang, Li Qian, Zhang Zhidong, Wang Dayong, Lan Lan, Zhang Jingxin, Zhao Yali, Wang Qiuju

Abstract excerpt

OBJECTIVE: Previous epidemiological studies indicate that GJB2, SLC26A4 or mtDNA 12S rRNA mutations were chiefly responsible for the hearing loss in children. A cost-effective method for screening deafness-associated mutations at early age is needed. This study aimed to develop a simple kit for screening of high risk deafness-associated mutations in newborns using tetra-primer amplification refractory mutation...

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Identifiers

PMID: 23815884
DOI: 10.1016/j.ijporl.2013.05.040

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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