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Article

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

Human molecular genetics - 1 Jul 1997

Woodward E R, Eng C, McMahon R, Voutilainen R, Affara N A, Ponder B A, Maher E R

Abstract excerpt

Inherited predisposition to phaeochromocytoma (MIM No 171300) occurs in multiple endocrine neoplasia type 2 (MEN 2) (MIM No 171400), von Hippel-Lindau (VHL) disease (MIM No 199300), and neurofibromatosis type 1 (NF1) (MIM No 162200). In addition, familial phaeochromocytoma alone has also been reported and we and others have identified germline VHL mutations in five of six kindreds analysed previously. Germline...

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Source

Identifiers

PMID: 9215674
DOI: 10.1093/hmg/6.7.1051

Genes

VHL
GDNF
RET

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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