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Article

Application of allele-specific primer extension-based microarray for simultaneous multi-gene mutation screening in patients with non-syndromic hearing loss.

International journal of molecular medicine - 1 Mar 2010

Choi Soo-Young, Lee Kyu-Yup, Kim Young-Eun, Bae Jae-Woong, Oh Se-Kyung, Kim So-Yeon, Hwang Sang-Joon, Kim Un-Kyung, Lee Sang-Heun

Abstract excerpt

Congenital hearing loss (HL) is the most common sensory disorder in humans, affecting one in 1000 infants at birth. A high degree of genetic heterogeneity makes it difficult to screen for mutations in all known deafness genes in clinical applications. We have improved a genotyping microarray usin...

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Source

Identifiers

PMID: 20127034
DOI: 10.3892/ijmm_00000347

Genes

GJB2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20127034-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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