Genetics of Parkinson disease
Open Access
- 1 December 2007
- journal article
- review article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 9 (12), 801-811
- https://doi.org/10.1097/gim.0b013e31815bf97c
Abstract
No abstract availableKeywords
This publication has 100 references indexed in Scilit:
- Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson diseaseMolecular Genetics and Metabolism, 2007
- Increased level of DJ-1 in the cerebrospinal fluids of sporadic Parkinson’s diseaseBiochemical and Biophysical Research Communications, 2006
- UCHL‐1 is not a Parkinson's disease susceptibility geneAnnals of Neurology, 2006
- DJ‐1 mutations and parkinsonism‐dementia‐amyotrophic lateral sclerosis complexAnnals of Neurology, 2005
- α-synuclein locus duplication as a cause of familial Parkinson's diseaseThe Lancet, 2004
- Genetic causes of Parkinson?s disease: UCHL-1Cell and tissue research, 2004
- Cysteine-106 of DJ-1 is the most sensitive cysteine residue to hydrogen peroxide-mediated oxidation in vivo in human umbilical vein endothelial cellsBiochemical and Biophysical Research Communications, 2004
- The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementiaAnnals of Neurology, 2003
- Case-control study of the ?-synuclein interacting protein gene and Parkinson's diseaseMovement Disorders, 2003
- Sequence Analysis of the Entire Mitochondrial Genome in Parkinson's DiseaseBiochemical and Biophysical Research Communications, 2002