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Article

A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.

BMC medical genetics - 30 Sept 2006

Thakur Nikita, Reddy D Nageshwar, Rao G Venkat, Mohankrishna P, Singh Lalji, Chandak Giriraj R

Abstract excerpt

BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare multi-organ cancer syndrome and understanding its genetic basis may help comprehend the molecular mechanism of familial cancer. A number of germ line mutations in the STK11 gene, encoding a serine threonine kinase have been reported in these pati...

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Identifiers

PMID: 17010210
DOI: 10.1186/1471-2350-7-73
PMCID: PMC1609100

Genes

STK11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17010210-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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