Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients

Germline mutations of the LKB1 (STK11) serine/threonine kinase gene (chromosome 19p13.3) cause Peutz-Jeghers syndrome, which is characterised by hamartomas of the gastrointestinal tract and typical pigmentation. Peutz-Jeghers syndrome carries an overall risk of cancer that may be up to 20 times that...

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Bibliografiska uppgifter
Huvudupphovsmän: Wang, Z, Churchman, M, Avizienyte, E, McKeown, C, Davies, S, Evans, D, Ferguson, A, Ellis, I, Xu, W., Yan, Z., Aaltonen, L, Tomlinson, I
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Group 1999
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Original Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734361/
https://ncbi.nlm.nih.gov/pubmed/10353780
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