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

Subjects

Subjects :

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

Details

Language :

English

ISSN :

1476-5551

Volume :

24

Issue :

1

Database :

MEDLINE

Journal :

Leukemia

Publication Type :

Report

Accession number :

19946261

Full Text :

https://doi.org/10.1038/leu.2009.210