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Article

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis.

Genomics - 1 Jan 2009

Ionita-Laza Iuliana, Rogers Angela J, Lange Christoph, Raby Benjamin A, Lee Charles

Abstract excerpt

Structural genetic variation, including copy-number variation (CNV), constitutes a substantial fraction of total genetic variability and the importance of structural genetic variants in modulating human disease is increasingly being recognized. Early successes in identifying disease-associated CN...

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Identifiers

PMID: 18822366
DOI: 10.1016/j.ygeno.2008.08.012
PMCID: PMC2631358

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18822366-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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