Mutations in STK11 gene in Czech Peutz-Jeghers patients

BACKGROUND: 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 (STK11) gene have been shown to be associated with the disease. Indi...

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Detalles Bibliográficos
Autores principales: Vasovčák, Peter, Puchmajerová, Alena, Roubalík, Jan, Křepelová, Anna
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2726128/
https://www.ncbi.nlm.nih.gov/pubmed/19615099
http://dx.doi.org/10.1186/1471-2350-10-69

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2726128/
https://www.ncbi.nlm.nih.gov/pubmed/19615099
http://dx.doi.org/10.1186/1471-2350-10-69

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