TransfusionHumansReceptorsThrombopoietinChromosomesHuman
Abnormal RH antigen expression in myeloid malignancies with MPL mutation, CSF3R mutation, or 1p deletion: Evidence of two distinct mechanisms.
Rémi Bourgeois, Laure Delanoe, Gauthier Alluin, Ludovic Firrera, Olivier Nibourel, Nicolas Duployez, Elisabeth Durieux-Roussel
Published: 202510.1111/trf.18482
Abstract
INTRODUCTION: RH phenotype abnormalities, such as double populations or the loss of antigen expression, are frequently observed in the laboratory, especially as a result of blood transfusions or hematopoietic stem cell transplantation. Less commonly,…
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