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...
Salvato in:
| Autori principali: | , , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Ferrata Storti Foundation
2005-01-01
|
| Serie: | Haematologica |
| Accesso online: | https://haematologica.org/article/view/3565 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|