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Application and progress of high-throughput sequencing technologies in the research of hereditary hearing loss.

Yi chuan = Hereditas - 20 Mar 2017

Wang Cui-cui, Yuan Hui-jun

Abstract excerpt

Hearing loss (HL) is the most common birth defect. Elucidating the genetic basis of hereditary deafness can not only assist diagnosis, provide the basis for genetic counseling and the prevention of deafness, but also bring a deeper understanding of the disease pathogenesis. In the genomic era, high-throughput sequencing technologies, represented by whole genome sequencing (WGS), whole exome sequencing (WES) or...

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PMID: 28420617
DOI: 10.16288/j.yczz.16-376

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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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