Mutations in <it>STK11 </it>gene in Czech Peutz-Jeghers patients

Mutations in <it>STK11 </it>gene in Czech Peutz-Jeghers patients

<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is an autosomal dominant hereditary disease characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis. The germline mutations in the serine/threonine kinase 11 (<it>ST...

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Bibliographic Details
Main Authors:	Křepelová Anna, Roubalík Jan, Puchmajerová Alena, Vasovčák Peter
Format:	Article
Language:	English
Published:	BMC 2009-07-01
Series:	BMC Medical Genetics
Online Access:	http://www.biomedcentral.com/1471-2350/10/69

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