8 results on '"Turnbull, Douglass M."'
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2. Maternally inherited mitochondrial DNA disease in consanguineous families
3. Respiratory chain complex I deficiency caused by mitochondrial DNA mutations
4. A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?
5. LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation
6. Noninvasive diagnosis of the 3243A>G mitochondrial DNA mutation using urinary epithelial cells
7. A novel point mutation in the mitochondrial tRNATrp gene produces a neurogastrointestinal syndrome
8. Leigh disease associated with a novel mitochondrial DNA ND5 mutation
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