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Article

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.

European journal of endocrinology - 1 Sept 2002

Villablanca Andrea, Wassif Wassif S, Smith Thomas, Höög Anders, Vierimaa Outi, Kassem Moustapha, Dwight Trisha, Forsberg Lars, Du Quan, Learoyd Diana, Jones Keston, Stranks Steve, Juhlin Claes, Teh Bin Tean, Carling Tobias, Robinson Bruce, Larsson Catharina

Abstract excerpt

BACKGROUND: Familial isolated hyperparathyroidism (FIHP) is a hereditary disorder characterised by uni- or multiglandular parathyroid disease. A subset of families are likely to be genetic variants of other familial tumour syndromes in which PHPT is the main feature, for example multiple endocrine neoplasia type 1 (MEN 1) and the hyperparathyroidism-jaw tumour syndrome (HPT-JT). OBJECTIVE: To investigate seven...

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Share to Chromosomes, Human, Pair 11
Share to Gene Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Germ-Line Mutation

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Share to Loss of Heterozygosity

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Source

Identifiers

PMID: 12213668
DOI: 10.1530/eje.0.1470313

Genes

MEN1

Variants

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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