C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies.

Staňo Kozubík, Kateřina

C-terminal RUNX1 mutation in familial platelet disorder with predisposition to myeloid malignancies. [electronic resource] - International journal of hematology Dec 2018 - 652-657 p. digital

Publication Type: Case Reports; Journal Article

1865-3774

10.1007/s12185-018-2514-3 doi


Biopsy
Blood Platelet Disorders--blood
Child, Preschool
Chromosome Aberrations
Core Binding Factor Alpha 2 Subunit--chemistry
DNA Mutational Analysis
Disease Progression
Family
Female
Genetic Predisposition to Disease
Humans
Karyotype
Leukemia, Myeloid--diagnosis
Mutation
Platelet Count
Polymorphism, Single Nucleotide