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Article

High-throughput sequencing to decipher the genetic heterogeneity of deafness.

Genome biology - 29 May 2012

Brownstein Zippora, Bhonker Yoni, Avraham Karen B

Abstract excerpt

Identifying genes causing non-syndromic hearing loss has been challenging using traditional approaches. We describe the impact that high-throughput sequencing approaches are having in discovery of genes related to hearing loss and the implications for clinical diagnosis.

Read the complete abstract on PubMed

Topics

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Share to Deafness
Share to Ear Surgery and Otitis Media
Share to Genetic Heterogeneity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing, Cochlea, Tinnitus, Genetics

Share to Hearing Loss

Share to Mutation

Share to Sequence Analysis, DNA

Source

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Identifiers

PMID: 22647651
DOI: 10.1186/gb-2012-13-5-245
PMCID: PMC3446284

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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