Our research aims to pioneer investigation into the interaction between inherited diseases, mitochondrial dysfunction, and type 2 diabetes from a genetic perspective within the Southern African population. We endeavour to contribute to the diagnosis and early detection of complex genomic diseases by enhancing analysis and diagnostic protocols, while reducing disease severity and improving quality of life for previously diagnosed patients.
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Complex Disease Genomics
AIM & MISSION
Follow these links for our main publications
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Principal Investigator
Students
- Ms Megan Collins (MSc)
- Ms Tiffany Clinton (MSc)
- Mr Craig Engelsman (Hons)
- Ms Robbyn Austin (Hons)
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Funders & research partners