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Article

Lessons from genes mutated in multiple endocrine neoplasia (MEN) syndromes.

Annales d'endocrinologie - 1 Jun 2005

Falchetti A, Marini Fr, Tonelli Fr, Brandi M L

Abstract excerpt

Multiple endocrine neoplasia (MEN) types 1 and 2 syndromes are rare hereditary cancer syndromes expressing a variety of endocrine and non-endocrine neoplasias and lesions. The improving of both molecular and clinical genetics knowledge helps health care providers in the whole spectrum of the clinical managements of MEN patients. The MEN1 gene, a tumour suppressor gene, is responsible of MEN1 syndrome, and is...

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Identifiers

PMID: 15988380
DOI: 10.1016/s0003-4266(05)81751-2

Genes

MEN1
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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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