Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.
作者信息
Jongmans M C J, Kuiper R P, Carmichael C L, Wilkins E J, Dors N, Carmagnac A, Schouten-van Meeteren A Y N, Li X, Stankovic M, Kamping E, Bengtsson H, Schoenmakers E F P M, van Kessel A Geurts, Hoogerbrugge P M, Hahn C N, Brons P P, Scott H S, Hoogerbrugge N
出版信息
Leukemia. 2010 Jan;24(1):242-6. doi: 10.1038/leu.2009.210. Epub 2009 Oct 15.
PMID:19946261
Abstract
摘要
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