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Article

A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.

BMC medical genetics - 19 Mar 2014

Bai Haihua, Yang Xukui, Temuribagen, Guilan, Suyalatu, Narisu, Wu Huiguang, Chen Yujie, Liu Yangjian, Wu Qizhu

Abstract excerpt

BACKGROUND: The genetic basis of autosomal dominant nonsyndromic hearing loss is complex. Genetic factors are responsible for approximately 50% of cases with congenital hearing loss. However, no previous studies have documented the clinical phenotype and genetic basis of autosomal dominant nonsyndromic hearing loss in Mongolians. METHODS: In this study, we performed exon capture sequencing of a Mongolian family...

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Source

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Identifiers

PMID: 25008054
DOI: 10.1186/1471-2350-15-34
PMCID: PMC3994966

Genes

TECTA

Variants

Provenance

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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