Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
- 17 December 2008
- journal article
- Published by Springer Science and Business Media LLC in neurogenetics
- Vol. 10 (2), 145-150
- https://doi.org/10.1007/s10048-008-0166-9
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Hereditary optic neuropathies share a common mitochondrial coupling defectAnnals of Neurology, 2008
- Regulation of mitochondrial matrix volumeAmerican Journal of Physiology-Cell Physiology, 2007
- Functional characterisation of ganglioside-induced differentiation-associated protein 1 as a glutathione transferaseBiochemical and Biophysical Research Communications, 2006
- Case 18-2006New England Journal of Medicine, 2006
- Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial networkThe Journal of cell biology, 2005
- Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effectJournal of Medical Genetics, 2005
- Evolutionary and Structural Analyses of GDAP1, Involved in Charcot-Marie-Tooth Disease, Characterize a Novel Class of Glutathione Transferase-Related GenesMolecular Biology and Evolution, 2003
- Mitochondrial Fusion in Human Cells Is Efficient, Requires the Inner Membrane Potential, and Is Mediated by MitofusinsMolecular Biology of the Cell, 2002
- Molecular cell biology of Charcot-Marie-Tooth disease.neurogenetics, 2002
- The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A diseaseNature Genetics, 2001