Spectrum of abnormalities and clonal transformation in germline RUNX1 familial platelet disorder and a genomic comparative analysis with somatic RUNX1 mutations in MDS/MPN overlap neoplasms.
DiFilippo EC, Coltro G, Carr RM, Mangaonkar AA, Binder M, Khan SP, Rodriguez V, Gangat N, Wolanskyj A, Pruthi RK, Chen D, He R, Viswanatha DS, Lasho T, Finke C, Tefferi A, Pardanani A, Patnaik MM.
DiFilippo EC, et al. Among authors: khan sp.
Leukemia. 2020 Sep;34(9):2519-2524. doi: 10.1038/s41375-020-0752-x. Epub 2020 Feb 14.
Leukemia. 2020.
PMID: 32060405
No abstract available.