Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Leukemia. 2010 Jan;24(1):242-6. doi: 10.1038/leu.2009.210. Epub 2009 Oct 15.

Authors

M C J Jongmans, R P Kuiper, C L Carmichael, E J Wilkins, N Dors, A Carmagnac, A Y N Schouten-van Meeteren, X Li, M Stankovic, E Kamping, H Bengtsson, E F P M Schoenmakers, A Geurts van Kessel, P M Hoogerbrugge, C N Hahn, P P Brons, H S Scott, N Hoogerbrugge

PMID: 19946261
DOI: 10.1038/leu.2009.210

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Blood Platelet Disorders / diagnosis
Blood Platelet Disorders / genetics*
Child
Child, Preschool
Core Binding Factor Alpha 2 Subunit / genetics*
Female
Gene Deletion
Humans
Leukemia, Myeloid, Acute / diagnosis
Leukemia, Myeloid, Acute / genetics*
Male
Mutation*

Substances

Core Binding Factor Alpha 2 Subunit
RUNX1 protein, human