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Article

Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations.

Frontiers in endocrinology - 1 Jan 2020

Mele Chiara, Mencarelli Monica, Caputo Marina, Mai Stefania, Pagano Loredana, Aimaretti Gianluca, Scacchi Massimo, Falchetti Alberto, Marzullo Paolo

Abstract excerpt

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs). MEN1 is usually consequent to different germline and somatic mutations of the MEN1 tumor suppressor gene, although phenocopies have also been reported. This review analyzed main biomedical databases searching for...

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Identifiers

PMID: 33312161
DOI: 10.3389/fendo.2020.591501
PMCID: PMC7708377

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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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