A novel <it>de novo </it>mutation in the serine-threonine kinase <it>STK11 </it>gene in a Korean patient with Peutz-Jeghers syndrome
<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is an unusual autosomal dominant disorder characterized by mucocutaneous pigmentation and multiple gastrointestinal hamartomatous polyps. Patients with PJS are at an increased risk of developing multi-org...
| Үндсэн зохиолчид: | , , , , , , , |
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| Формат: | Өгүүллэг |
| Хэл сонгох: | English |
| Хэвлэсэн: |
BMC
2008-05-01
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| Цуврал: | BMC Medical Genetics |
| Онлайн хандалт: | http://www.biomedcentral.com/1471-2350/9/44 |