Failure to find mutations in ubiquitin carboxy-terminal hydrolase L1 gene in familial Parkinson's disease
- 31 October 2000
- journal article
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 6 (4) , 199-200
- https://doi.org/10.1016/s1353-8020(00)00022-5
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
- National Parkinson Foundation
- University of Miami
This publication has 5 references indexed in Scilit:
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- The ubiquitin pathway in Parkinson's diseaseNature, 1998
- Substrate Specificity of Deubiquitinating Enzymes: Ubiquitin C-Terminal HydrolasesBiochemistry, 1998
- A clinical and genetic study of familial Parkinson's diseaseMovement Disorders, 1991
- Ubiquitin carboxyl‐terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseasesThe Journal of Pathology, 1990