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Cancer risks in LKB1 germline mutation carriers
BACKGROUND AND AIMS: Germline mutations in the LKB1 gene are known to cause Peutz‐Jeghers syndrome, which is an autosomal dominant disorder characterised by hamartomatous polyposis and mucocutaneous pigmentation. This syndrome is associated with an increased risk of malignancies in different organs...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1856321/ https://ncbi.nlm.nih.gov/pubmed/16407375 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2005.082990 |
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