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Article

Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program.

Annals of human genetics - 1 Sept 2008

Hu Y, Li L, Seidelmann S B, Timur A A, Shen P H, Driscoll D J, Wang Q K

Abstract excerpt

Klippel-Trenaunay syndrome (KTS) is a severe congenital disorder characterized by capillary malformations, venous malformations or varicose veins, and hypertrophy of the affected tissues. The angiogenic factor gene AGGF1 was previously identified as a candidate susceptibility gene for KTS, but fu...

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Identifiers

PMID: 18564129
DOI: 10.1111/j.1469-1809.2008.00458.x
PMCID: PMC2602961

Genes

AGGF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18564129-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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