Screening for VPS35 mutations in Parkinson's disease
Open Access
- 30 April 2012
- journal article
- research article
- Published by Elsevier in Neurobiology of Aging
- Vol. 33 (4) , 838.e1-838.e5
- https://doi.org/10.1016/j.neurobiolaging.2011.10.032
Abstract
No abstract availableKeywords
Funding Information
- Medical Research Council and Wellcome Trust Disease Centre (WT089698/Z/09/Z)
This publication has 26 references indexed in Scilit:
- Olfactory dysfunction in LRRK2 G2019S mutation carriersNeurology, 2011
- A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson DiseasePublished by Elsevier ,2011
- Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1Science, 2004
- Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson diseaseNeurology, 2004
- Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptorThe Journal of cell biology, 2004
- Staging of brain pathology related to sporadic Parkinson’s diseaseNeurobiology of Aging, 2003
- Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset ParkinsonismScience, 2003
- Mutation in the α-Synuclein Gene Identified in Families with Parkinson's DiseaseScience, 1997
- The Frequency of Idiopathic Parkinson's Disease by Age, Ethnic Group, and Sex in Northern Manhattan, 1988–1993American Journal of Epidemiology, 1995
- Development of the university of pennsylvania smell identification test: A standardized microencapsulated test of olfactory functionPhysiology & Behavior, 1984