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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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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2009
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| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2726128/ https://ncbi.nlm.nih.gov/pubmed/19615099 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-69 |
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