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Article

Detection of mutations in genes associated with hearing loss using a microarray-based approach.

The Journal of molecular diagnostics : JMD - 1 Sept 2006

Siemering Kirby, Manji Shehnaaz S M, Hutchison Wendy M, Du Sart Desiree, Phelan Dean, Dahl Hans-Henrik M

Abstract excerpt

Knowing the etiology of hearing loss in a person has implications for counseling and management of the condition. More than 50% of cases of early onset, nonsyndromic sensorineural hearing loss are attributable to genetic factors. However, deafness is a genetically heterogeneous condition and it is therefore currently not economically and practically feasible to screen for mutations in all known deafness genes. We...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16931589
DOI: 10.2353/jmoldx.2006.050147
PMCID: PMC1867613

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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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