Mutations in <it>STK11 </it>gene in Czech Peutz-Jeghers patients
<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is an autosomal dominant hereditary disease characterized by mucocutaneous pigmentation and gastrointestinal hamartomatous polyposis. The germline mutations in the serine/threonine kinase 11 (<it>STK11</it>) gene have been shown to be...
Kaydedildi:
| Asıl Yazarlar: | , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2009-07-01
|
| Seri Bilgileri: | BMC Medical Genetics |
| Online Erişim: | http://www.biomedcentral.com/1471-2350/10/69 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|