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Updated: May 10, 2025

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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Exploring pharmacogenetic factors influencing hydroxyurea response in tanzanian sickle cell disease patients: a

Siana Nkya1,2,3,4, Collin Nzunda5, Emmanuel Saukiwa2

  • 1Department of Haematology and Blood Transfusion,, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

The Pharmacogenomics Journal
|April 23, 2025
PubMed

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