Mitochondrial disorders
- 9 February 1999
- journal article
- editorial
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Vol. 1410 (2) , 99-102
- https://doi.org/10.1016/s0005-2728(98)00160-1
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Biochemical abnormalities and excitotoxicity in Huntington's disease brainAnnals of Neurology, 1999
- The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathyAnnals of Neurology, 1998
- Localization of the Wilson’s disease protein product to mitochondriaProceedings of the National Academy of Sciences, 1998
- Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) SubunitAmerican Journal of Human Genetics, 1998
- Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal gangliaAnnals of Neurology, 1997
- Mitochondrial defect in Huntington's disease caudate nucleusAnnals of Neurology, 1996
- Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyNature Genetics, 1995
- Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.Proceedings of the National Academy of Sciences, 1995
- Mitochondrial function and parental sex effect in Huntington's diseaseThe Lancet, 1990
- Mitochondrial Myopathy with a Defect of Mitochondrial-Protein TransportNew England Journal of Medicine, 1990