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    • A metabolomics investigation of selected m.3243A>G mutation phenotypes 

      Esterhuizen, K. (North-West University, 2018)
      Mitochondrial disease (MD) is a subgroup of inborn errors of metabolism, which can be caused by a mutation in either the nuclear DNA (nDNA) or mitochondrial DNA (mtDNA). One of the most common mtDNA disease causing mutations ...