Inborn errors of complex II – Unusual human mitochondrial diseases
- 2 December 2001
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Vol. 1553 (1-2) , 117-122
- https://doi.org/10.1016/s0005-2728(01)00228-6
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Repositioning the hereditary paraganglioma critical region on chromosome band 11q23Human Genetics, 1999
- Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxiaNature Genetics, 1997
- A Chinese Hamster Mutant Cell Line with a Defect in the Integral Membrane Protein CII-3 of Complex II of the Mitochondrial Electron Transport ChainPublished by Elsevier ,1995
- Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencyNature Genetics, 1995
- The cDNA sequence of the flavoprotein subunit of human heart succinate dehydrogenaseBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1994
- Single Muscle Fibre Analyses in 2 Brothers with Succinate Dehydrogenase DeficiencyEuropean Neurology, 1994
- The gene for the iron sulfur protein of succinate dehydrogenase (SDH-IP) maps to human chromosome 1p35-36.1Somatic Cell and Molecular Genetics, 1993
- Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with leigh syndromeBrain & Development, 1992
- Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.Journal of Clinical Investigation, 1991
- Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathyBiochemical and Biophysical Research Communications, 1989