Associated Papers
Increased blood-derived mitochondrial DNA copy number in African ancestry individuals with Parkinson's disease.
Müller-Nedebock AC et al.
Parkinsonism & Related Disorders, 2022
Mitochondrial molecular genetic results in a South African cohort: divergent mitochondrial and nuclear DNA findings.
Meldau S et al.
Journal of Clinical Pathology, 2022
Natural History of Leigh Syndrome: A Study of Disease Burden and Progression.
Lim AZ et al.
Annals of Neurology, 2022
A case for genomic medicine in South African paediatric patients with neuromuscular disease.
Raga SV et al.
Frontiers in Pediatrics, 2022
Identification of a single MPV17 nonsense-associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy.
Meldau S et al.
Clinical Genetics, 2018
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