Φορτώνει......
Role of Lkb1, the causative gene of Peutz–Jegher's syndrome, in embryogenesis and polyposis
Peutz–Jeghers syndrome (PJS) is a dominantly inherited human disorder characterized by gastrointestinal hamartomatous polyposis and mucocutaneous melanin pigmentation. LKB1 (STK11) serine/threonine kinase is the product of the causative gene of PJS, which has been mapped to chromosome 19p13.3. Howev...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
National Academy of Sciences
2002
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC124396/ https://ncbi.nlm.nih.gov/pubmed/12060709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.122254599 |
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