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

✍ Scribed by 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

• Book ID: 109886963
• Publisher: Nature Publishing Group
• Year: 2009
• Tongue: English
• Weight: 187 KB
• Volume: 24
• Category: Article
• ISSN: 0887-6924
• DOI: 10.1038/leu.2009.210