Abstract
In this issue of Blood, Vincent et al report on their seminal finding of the contribution of mast cell activation to neurogenic inflammation, and thus to the pathobiology of pain in sickle cell disease (SCD).1 © 2013 by The American Society of Hematology.
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CITATION STYLE
APA
Kutlar, A. (2013, September 12). GLEE-ful for sickle cell pain? Blood. American Society of Hematology. https://doi.org/10.1182/blood-2013-07-510982
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