Mitochondrial ND5 mutations in idiopathic Parkinson’s disease
- 1 January 2005
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 326 (3), 667-669
- https://doi.org/10.1016/j.bbrc.2004.11.093
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- High frequency of mitochondrial complex I mutations in Parkinson’s disease and agingNeurobiology of Aging, 2004
- Parkinson's disease transgenic mitochondrial cybrids generate Lewy inclusion bodiesJournal of Neurochemistry, 2004
- Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiencyJournal of Medical Genetics, 2003
- Is the mitochondrial complex I ND5 gene a hot‐spot for MELAS causing mutations?Annals of Neurology, 2002
- Leigh disease associated with a novel mitochondrial DNA ND5 mutationEuropean Journal of Human Genetics, 2002
- Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's diseaseAnnals of Neurology, 1998
- Mitochondrial Dysfunction in Idiopathic Parkinson DiseaseAmerican Journal of Human Genetics, 1998
- Origin and functional consequences of the complex I defect in Parkinson's diseaseAnnals of Neurology, 1996
- Abnormalities of the electron transport chain in idiopathic parkinson's diseaseAnnals of Neurology, 1989
- MITOCHONDRIAL COMPLEX I DEFICIENCY IN PARKINSON'S DISEASEThe Lancet, 1989