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Updated: Mar 2, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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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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SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from

Gift Dineo Pule1, Valentina Josiane Ngo Bitoungui2, Bernard Chetcha Chemegni2

  • 1Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Anzio Road, Observatory, Cape Town, 7925, Republic of South Africa.

BMC Research Notes
|May 14, 2017
PubMed

Keywords:
CameroonFetal hemoglobinSAR1a promoterSickle cell disease

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