Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome

Br J Haematol. 2009 May;145(4):533-4. doi: 10.1111/j.1365-2141.2009.07634.x.

Authors

Doris Steinemann¹, Inka Praulich, Noreen Otto, Gudrun Göhring, Charlotte M Niemeyer, Brigitte Schlegelberger

Affiliation

¹ Institute of Cell and Molecular Pathology, Hannover Medical School, Hannover, Germany. [email protected]

PMID: 19298594
DOI: 10.1111/j.1365-2141.2009.07634.x

No abstract available

MeSH terms

Adaptor Proteins, Signal Transducing
Adolescent
Child
DNA Mutational Analysis
Female
Humans
Male
Myelodysplastic Syndromes / genetics*
Myelodysplastic Syndromes / pathology
Polymorphism, Single Nucleotide*
Proteins / genetics*

Substances

Adaptor Proteins, Signal Transducing
HAX1 protein, human
Proteins