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Gene4HL: An Integrated Genetic Database for Hearing Loss

18 Oct 2021

Abstract excerpt

Hearing loss (HL) is one of the most common disabilities in the world. In industrialized countries, HL occurs in 1-2/1,000 newborns, and approximately 60% of HL is caused by genetic factors. Next generation sequencing (NGS) has been widely used to identify many candidate genes and variants in patients with HL, but the data are scattered in multitudinous studies. It is a challenge for scientists, clinicians, and...

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PMID: 34733322
DOI: 10.3389/fgene.2021.773009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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