Similar Items: Mitochondrial DNA (mtDNA) mutations in patients with suspected myoclonic epilepsy and ragged red muscle fibres (MERRF), Leigh syndrome (LS), and mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
- Mitochondrial encephalomyopathies : an analysis of clinical and laboratory data of patients at the Red Cross Children's Hospital
- Quantifying admixture in the Afrikaner population using mitochondrial DNA
- Systematic relationships in southern African Francolins as determined from mitochondrial DNA
- Investigating mitochondrial DNA mutations driving dysfunction and intervertebral disc degeneration
- Investigating mitochondrial DNA sequence variation and copy number in individuals of African ancestry living with Parkinson’s disease.
- Systematics of cetaceans using restriction site mapping of mitochondrial DNA
Author: Olckers, Antonel
- Mitochondrial DNA (mtDNA) mutations in patients with suspected myoclonic epilepsy and ragged red muscle fibres (MERRF), Leigh syndrome (LS), and mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)
- Screening for specific mutations in malignant hyperthermia susceptible families
- Genetic heterogeneity in South African facioscapulohumeral muscular dystrophy (FSHD) families