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Article

MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1.

European journal of endocrinology - 1 Feb 2000

Morelli A, Falchetti A, Martineti V, Becherini L, Mark M, Friedman E, Brandi M L

Abstract excerpt

Multiple endocrine neoplasia type 1 (MEN 1) is a familial syndrome characterized by parathyroid, enteropancreatic and pituitary tumors. The gene responsible for this syndrome is localized at chromosomal 11q13 region and DNA markers from this region cosegregate with the disease. The recent identification of the MEN1 gene, encoding for a protein termed menin of 610 amino acids, allowed mutational screening to be...

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Source

Identifiers

PMID: 10664520
DOI: 10.1530/eje.0.1420131

Genes

MEN1

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening.Semantic proximity Read ↗

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