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Article

Contribution of genetic analysis in screening for MEN1 among patients with sporadic disease and one or more typical manifestation.

Annales d'endocrinologie - 1 Dec 2006

Odou M-F, Cardot-Bauters C, Vantyghem M-C, Carnaille B, Leteurtre E, Pigny P, Verier-Mine O, Desailloud R, Porchet N

Abstract excerpt

Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant hereditary syndrome (OMIM 131100) due to MEN1 gene mutations, predisposing to the development of hyperplasic and tumoral lesions of neuroendocrine tissues. Since the identification of the gene in 1997, more than 400 different mutations of MEN1 have been registered. Genotypic analysis of MEN1 remains fastidious and must be reserved to targeted...

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Share to Chromosomes, Human, Pair 11
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17194968
DOI: 10.1016/s0003-4266(06)73010-4

Genes

MEN1

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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