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Article

VHL gene mutation analysis of a Chinese family with non- syndromic pheochromocytomas and patients with apparently sporadic pheochromocytoma.

Asian Pacific journal of cancer prevention : APJCP - 1 Jan 2015

Zhang Bin, Qian Jing, Chang De-Hui, Wang Yang-Min, Zhou Da-Hai, Qiao Gou-Mei

Abstract excerpt

OBJECTIVE: The Von Hippel-Lindau syndrome (VHLD), an inherited neoplastic syndrome predisposing to central nervous system hemangioblastoma (CNS), pheochromocytoma (PCC), renal cell carcinoma(RCC), retinal hemangioma (RA) and renal cysts, is caused by mutations or deletions of the VHL tumor-suppressor gene. To assess VHL genotype-phenotype correlations with function of pVHL a gene mutation analysis of members in a...

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Source

Identifiers

PMID: 25773797
DOI: 10.7314/apjcp.2015.16.5.1977

Genes

VHL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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