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Article

Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.

Human genetics - 1 Jan 2009

Connell F C, Ostergaard P, Carver C, Brice G, Williams N, Mansour S, Mortimer P S, Jeffery Steve

Abstract excerpt

Milroy disease (hereditary lymphoedema type I, MIM 153100) is a congenital onset primary lymphoedema with autosomal dominant inheritance. Mutations in the gene, vascular endothelial growth factor receptor 3, VEGFR3 (FLT4), are known to cause Milroy disease, but there is uncertainty about the prev...

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Source

Identifiers

PMID: 19002718
DOI: 10.1007/s00439-008-0586-5

Genes

VEGFC
FLT4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19002718-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas.PMID 19002718Read ↗

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