Low frequency of the glutathione-S-transferase T1-null genotype in patients with primary myelodysplastic syndrome and 5q deletion

Leukemia. 2008 Aug;22(8):1643-6. doi: 10.1038/leu.2008.35. Epub 2008 Feb 28.

Authors

C Stavropoulou, C Sambani, H Rigana, V N Georgakakos, G Voutsinas, K N Manola, G E Pantelias, V Makropoulos; Hellenic MDS Study Group

Collaborators

Hellenic MDS Study Group:
A Symeonidis, A Kouraklis, N C Zoumbos, N Viniou, E Plata, A G Galanopoulos, T Marinakis, N I Anagnostopoulos, P Roussou, A Fragou, A Parcharidou, V Pappa, A Lazaridou, C Mitsouli, C Megalakaki, M Bakiri, M Papaioannou, N Laoutaris, H A Papadaki, G Bourikas, M Protopappa, D Georgiadou, P Zikos

PMID: 18305556
DOI: 10.1038/leu.2008.35

No abstract available

Publication types

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

MeSH terms

Chromosome Deletion*
Chromosomes, Human, Pair 5*
Genotype
Glutathione Transferase / genetics*
Humans
Myelodysplastic Syndromes / genetics*

Substances

Glutathione Transferase