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Article

Analysis of STK11 gene variant in five Chinese patients with Peutz-Jeghers syndrome.

Digestive diseases and sciences - 1 Oct 2013

Zheng Bixia, Pan Jian, Wang Yaping, Li Mei, Lian Min, Zheng Yucan, Jin Yu

Abstract excerpt

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant inherited disorder characterized by gastrointestinal hamartomatous polyps and mucocutaneous pigmentation. Germline mutation of a serine/threonine kinase 11(STK11) gene has been identified as a cause of PJS. In this study, we investigated the molecular basis of five Chinese PJS patients. METHODS: Blood samples were collected from five unrelated...

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Source

Identifiers

PMID: 23892522
DOI: 10.1007/s10620-013-2737-3

Genes

STK11

Variants

Provenance

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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