Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia
Open Access
- 20 February 2004
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 124 (6) , 843-844
- https://doi.org/10.1111/j.1365-2141.2004.04862.x
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- Regulation of the Mitogen-activated Protein Kinase Signaling Pathway by SHP2Journal of Biological Chemistry, 2002
- Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndromeNature Genetics, 2001
- Structure and function of SH2-domain containing tyrosine phosphatasesSeminars in Cell Biology, 1993