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High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients
BACKGROUND: Peutz-Jeghers syndrome (PJS) is a rare autosomal dominantly inherited disease characterized by gastrointestinal hamartomatous polyposis and mucocutaneous pigmentation. The genetic predisposition for PJS has been shown to be associated with germline mutations in the STK11/LKB1 tumor suppr...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3012662/ https://ncbi.nlm.nih.gov/pubmed/21118512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-169 |
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