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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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BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

P Sebastiani1, J J Farrell2, A Alsultan3

  • 1Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States.

Blood Cells, Molecules & Diseases
|February 24, 2015
PubMed
Abstract

Keywords:
Genetic associationHaplotype analysisHemoglobinSickle cell disease

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