Alex Bismark Atta-Owusu

ORCID: 0009-0007-4289-7732
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About
Contact & Profiles
Research Areas
  • Hemoglobinopathies and Related Disorders
  • Sleep and related disorders
  • Sleep and Work-Related Fatigue
  • Iron Metabolism and Disorders
  • Sleep and Wakefulness Research

University of Cape Coast
2025

Sickle cell disease (SCD) is a genetic disorder with diverse spectrum of clinical presentation, often determined by inherited βS gene haplotypes. Ghana, country significant SCD burden, lacks population haplotype frequency data, hindering anthropological, genetic, and understanding management the disease. A prospective sample 191 patients (sickle anemia; homozygous HbSS) was recruited at Korle-Bu Teaching Hospital, Accra. Identification haplotypes performed using polymerase chain...

10.1080/03630269.2025.2474609 article EN Hemoglobin 2025-03-05
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