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Article

Molecular diagnostics for hereditary hearing loss in children.

Expert review of molecular diagnostics - 1 Aug 2017

Sommen Manou, Wuyts Wim, Van Camp Guy

Abstract excerpt

INTRODUCTION: Hearing loss (HL) is the most common birth defect in industrialized countries with far-reaching social, psychological and cognitive implications. It is an extremely heterogeneous disease, complicating molecular testing. The introduction of next-generation sequencing (NGS) has resulted in great progress in diagnostics allowing to study all known HL genes in a single assay. The diagnostic yield is...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28593790
DOI: 10.1080/14737159.2017.1340834

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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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