Haptoglobin genotype predicts severe acute vaso-occlusive pain episodes in children with sickle cell anemia

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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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Shaina M Willen1, Joel Brennan McNeil2, Mark Rodeghier3

  • 1Division of Pulmonary Medicine, Department of Pediatrics, UCSF Benioff Children's Hospital San Francisco, San Francisco, California.

American Journal of Hematology
|January 11, 2020
PubMed
Abstract

No abstract available in PubMed .

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