A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population-Reference-Cited by-同舟云学术

A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population

Published:2001-08 Issue:1-2 Volume:189 Page:113-117
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Satoh Jun-ichi,Kuroda Yasuo

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Etiology and pathogenesis of Parkinson's disease;Olanow;Annu. Rev. Neurosci.,1999

2. The genetics of Parkinson's disease;de Silva;Curr. Opin. Genet. Dev.,2000

3. Variability and validity of polymorphism association studies in Parkinson's disease;Tan;Neurology,2000

4. Roles of ubiquitinylation in proteolysis and cellular regulation;Wilkinson;Ann. Rev. Nutr.,1995

5. Ubiquitin, cellular inclusions and their role in neurodegeneration;Alves-Rodrigues;Trends Neurosci.,1998

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