Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson's disease
- 25 September 2006
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 247 (2) , 224-230
- https://doi.org/10.1016/j.jns.2006.05.053
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- EPIDEMIOLOGY OF PARKINSON'S DISEASEPublished by Elsevier ,2005
- Inhibition of NADH-linked oxidation in brain mitochondria by 1-methyl-4-phenyl-pyridine, a metabolite of the neurotoxin, 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridinePublished by Elsevier ,2002
- Mitochondrial DNA A4336G Mutation in Alzheimer’s and Parkinson’s DiseasesEuropean Neurology, 2002
- Familial aggregation of Parkinson's disease in a Finnish populationJournal of Neurology, Neurosurgery & Psychiatry, 2000
- Genotype in the 24-kDa Subunit Gene (NDUFV2) of Mitochondrial Complex I and Susceptibility to Parkinson DiseaseGenomics, 1998
- Gerstmann-Straussler-Scheinker disease in an Alsatian family: clinical and genetic studies.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Chronic Parkinsonism in Humans Due to a Product of Meperidine-Analog SynthesisScience, 1983
- Sequence and organization of the human mitochondrial genomeNature, 1981
- PARKINSON'S DISEASEBrain, 1973