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Article

Genetic screening of 15 hearing loss variants in 77,647 neonates with clinical follow-up.

Molecular genetics & genomic medicine - 1 Jan 2024

Kun Lin, Jiexiang Huang, Hua Lin, Junlin Han, Yijun Ruan, Lixian Zhang, Mingqiao Chen

Abstract excerpt

BACKGROUND: To analyze the genotype distribution and frequency of hearing loss genes in newborn population and evaluate the clinical value of genetic screening policy in China. METHODS: Genetic screening for hearing loss was offered to 84,029 neonates between March 2019 and December 2021, of whom 77,647 newborns accepted the screening program with one-year follow-up. The genotyping of 15 hot spot variants in...

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Identifiers

PMID: 38037722
DOI: 10.1002/mgg3.2324
PMCID: PMC10767602

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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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