Mutations of PTPN11 are rare in adult myeloid malignancies
The PTPN11 gene encodes the phospho-tyrosyine phosphatase protein SHP-2. Constitutional mutations of this gene are involved in Noonan's syndrome, a developmental disorder in which children have a predisposition to develop a myeloid disorder called juvenile myelomonocytic leukemia. Recently, studies...
Збережено в:
| Автори: | , , , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Ferrata Storti Foundation
2005-01-01
|
| Серія: | Haematologica |
| Онлайн доступ: | https://haematologica.org/article/view/3565 |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|