LKB1/ STK11, Peutz-Jeghers syndrome and cancer. Introduction
- PMID: 21874563
- PMCID: PMC3175341
- DOI: 10.1007/s10689-011-9474-6
LKB1/ STK11, Peutz-Jeghers syndrome and cancer. Introduction
References
-
- Peutz JLA. Over een zeer merkwaardige, gecombineerde familiaire polyposis van de slijmvliezen van den tractus intestinalis met die van de neuskeelholte en gepaard met eigenaardige pigmentaties van huid en slijmvliezen. Ned Maandschr Geneeskd. 1921;10:134–146.
-
- Jeghers H, McKusick VA, Katz KH (1949) Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits. A syndrome of diagnostic significance. N Engl J Med 241:993–1005, 1031–1036 - PubMed
-
- Hemminki A, Markie D, Tomlinson I et al (1998) A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391:184–187 - PubMed
-
- Jenne DE, Reimann H, Nezu J (1998) Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nature Genet 18:38–43 - PubMed
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