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Article

Unveiling a novel GJB2 dominant K22T mutation in a Chinese family with hearing loss.

Acta biochimica et biophysica Sinica - 25 Jun 2024

Ji Haiting, Shu Yilai, Li Huawei

Abstract excerpt

Hearing loss constitutes one of the most prevalent conditions within the field of otolaryngology. Recent investigations have revealed that mutations in deafness-associated genes, including point mutations and variations in DNA sequences, can cause hearing impairments. With the ethology of deafness remaining unclear for a substantial portion of the affected population, further screenings for pathogenic mutations...

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Identifiers

PMID: 38733163
DOI: 10.3724/abbs.2024064
PMCID: PMC11292126

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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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