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Article

Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.

World journal of gastroenterology - 14 Nov 2009

Ausavarat Surasawadee, Leoyklang Petcharat, Vejchapipat Paisarn, Chongsrisawat Voranush, Suphapeetiporn Kanya, Shotelersuk Vorasuk

Abstract excerpt

Peutz-Jeghers syndrome (PJS), a rare autosomal dominant inherited disorder, is characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome have a predisposition to a variety of cancers in multiple organs. Mutations in the serine/threonine kin...

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Source

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Identifiers

PMID: 19908348
DOI: 10.3748/wjg.15.5364
PMCID: PMC2776867

Genes

STK11

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19908348-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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