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Article

A large Turkish pedigree with multiple endocrine neoplasia type 1 syndrome carrying a rare mutation: c.1680_1683 del TGAG.

The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology - 1 Jul 2020

Demirtaş Coşkun Özer, Ata Pınar, Çetin Ali, Türkyılmaz Ayberk, Duman Deniz Guney

Abstract excerpt

BACKGROUND AND AIMS: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome characterized by tumors arising from endocrine glands with no specific genotype-phenotype correlation. Herein, we report the largest Turkish kindred with MEN1 inherited a scarce MEN1 mutation gene. MATERIALS AND METHODS: Sixty-four year-old man, referred to our gastroenterology outpatient clinic for evaluation of...

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Identifiers

PMID: 32897224
DOI: 10.5152/tjg.2020.19830
PMCID: PMC7480197

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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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