A novel mutation in <it>STK11 </it>gene is associated with Peutz-Jeghers Syndrome in Indian patients
<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is a rare multi-organ cancer syndrome and understanding its genetic basis may help comprehend the molecular mechanism of familial cancer. A number of germ line mutations in the <it>STK11 </it>gene, encoding a serine threonine kinase h...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2006-09-01
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| Col·lecció: | BMC Medical Genetics |
| Accés en línia: | http://www.biomedcentral.com/1471-2350/7/73 |
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