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Article

Variant analysis of 92 Chinese Han families with hearing loss.

BMC medical genomics - 21 Jan 2022

Jin Xiaohua, Huang Shasha, An Lisha, Zhang Chuan, Dai Pu, Gao Huafang, Ma Xu

Abstract excerpt

BACKGROUND: Hearing loss (HL) is the most frequent sensory deficit in humans, HL has strong genetic heterogeneity. The genetic diagnosis of HL is very important to aid treatment decisions and to provide prognostic information and genetic counseling for the patient's family. METHODS: We undertook pedigree analysis in 92 Chinese non-syndromic HL patients by targeted next-generation sequencing and Sanger sequencing....

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Identifiers

PMID: 35062939
DOI: 10.1186/s12920-022-01158-3
PMCID: PMC8781451

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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