A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.

We describe a patient with acquired alpha-thalassemia myelodysplastic syndrome (ATMDS). A previously healthy 66-year-old man presented with hemoglobin of 9.3 g/dL, mean corpuscular volume 59 fL, and a bone marrow aspirate with increased erythroid precursors and hypolobulated megakaryocytes. Hemoglob...

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Main Authors: Costa, D, Fisher, C, Miller, K, Pihan, G, Steensma, D, Gibbons, R, Higgs, D
Formato: Journal article
Idioma:English
Publicado em: 2006