Inositide-specific phospholipase c beta1 gene deletion is a rare event in myelodysplastic syndromes.

Adult; Aged; Aged, 80 and over; Female; Gene Deletion; Humans; Inositol/metabolism; Isoenzymes/genetics; Male; Middle Aged; Myelodysplastic Syndromes/enzymology/genetics; Phospholipase C beta; Type C Phospholipases/genetics

Disciplines :

Hematology
Genetics & genetic processes

Author, co-author :

Herens, Christian ; Centre Hospitalier Universitaire de Liège - CHU > Génétique

Ketelslegers, O.

Tassin, Françoise ; Centre Hospitalier Universitaire de Liège - CHU > Hématologie biologique et immuno hématologie

Hansen, S.; Centre Hospitalier Universitaire de Liège - CHU > Génétique

Bours, Vincent ; Centre Hospitalier Universitaire de Liège - CHU > Génétique

Language :

English

Title :

Inositide-specific phospholipase c beta1 gene deletion is a rare event in myelodysplastic syndromes.

Publication date :

2006

Journal title :

Leukemia

ISSN :

0887-6924

eISSN :

1476-5551

Publisher :

Nature Publishing Group, London, United Kingdom

Volume :

Issue :

Pages :

521-2; author reply 522-3

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 02 February 2010

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Bibliography

Steensma DP, Tefferi A. The myelodysplastic syndrome(s): A perspective and review highlightening current controversies. Leuk Res 2003; 27: 95-120.
Lo Vasco VR, Calabrese G, Manzoli L, Palka G, Spadano A, Morizio E et al. Inositide-specific phospholipase c β1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukaemia. Leukemia 2004; 18: 1122-1126.