Now showing items 1-2 of 2

    • Control of alkaptonuria with nitisinone and gene therapy: A systematic review 

      Martin L., Nelwan (African Science Publications, 2021-01-01)
      Alkaptonuria (AKU) is a genetic disorder inherited in accordance with Mendel first law. Mutations in the HGA gene result in the AKU disorder. Three major features of this disorder: arthritis, ochronosis, and the presence ...
    • Phenylketonuria: Genes in phenylketonuria, diagnosis, and treatments 

      Martin L., Nelwan (African Journal of Biological Sciences, 2020-01-01)
      Introduction: Phenylketonuria (PKU) is a rare autosomal-recessive disorder inherited in accordance with the law of segregation. Detection tools for people with PKU can include Sanger Sequencing (SS) and Next Generation ...