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Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome
Peutz-Jeghers syndrome (PJS), a rare autosomal dominant inherited disorder, is characterized by hamartomatous gastrointestinal polyps and mucocutaneous pigmentation. Patients with this syndrome have a predisposition to a variety of cancers in multiple organs. Mutations in the serine/threonine kinase...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The WJG Press and Baishideng
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2776867/ https://ncbi.nlm.nih.gov/pubmed/19908348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.15.5364 |
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