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Published in 2020 at "Pediatric Research"
DOI: 10.1038/s41390-020-01213-8
Abstract: I have two sons with Sickle Hemoglobin E Disease (SE). They are caucasian-hispanic, both have a baseline hemoglobin in the 11–13 range with low reticulocytes, and yes, both have complications from chronic pain, vaso-occlusive crisis,…
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Keywords:
cell patient;
typically atypical;
atypical sickle;
sickle ... See more keywords