A novel mtDNA C11777A mutation in Leigh syndrome

Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

Douglas C. Wallace, Gurparkash Singh, Marie T. Lott et al. · Science · 1988 · 2.4K citations

Neurodegenerative Diseases, Ophthalmology, Biochemistry +14

Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by Complementation

Michael P. King, Giuseppe Attardi · Science · 1989 · 1.6K citations

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

Trends in Genetics · 1990 · 1.4K citations

Mitochondrial Biogenesis, Mitochondrial Function, Human Cells +10

SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT

Denis Leigh · Journal of Neurology Neurosurgery & Psychiatry · 1951 · 780 citations · Full text

Neurological Disorder, Pediatrics, Brain Injury +4

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Thomas Bourgeron, Pierre Rustin, Dominique Chrétien et al. · Nature Genetics · 1995 · 723 citations

Mitochondrial Function, Biochemistry, Natural Sciences +9