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Article

Copy number variation in metabolic phenotypes.

Cytogenetic and genome research - 1 Jan 2008

Lanktree M, Hegele R A

Abstract excerpt

Despite successes in identifying genetic contributors to common metabolic phenotypes, only part of the heritable component of these traits has thus far been explained. Copy number variation (CNV) is likely to be responsible for some of the unexplained variation. As observed with single nucleotide changes, it is probable that both rare and common CNVs will contribute to susceptibility to metabolic disease. For...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

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Share to Hyperlipoproteinemia Type II

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Source

Identifiers

PMID: 19287152
DOI: 10.1159/000184705

Genes

LDLR
LPA

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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