Association of the ubiquitin carboxy-terminal hydrolase-L1 genetic polymorphism with the susceptibility of Parkinson's disease

Chinese Journal of Medical Genetics

Volumn 25, Issue 5, 2008, Pages 586-587

  Xiao, Ying ^a   Zhang, Ben Shu ^a  

^a TIANJIN MEDICAL UNIVERSITY   (China)

Author keywords

Association; Parkinson's disease; Ubiquitin carboxy terminal hydrolase L1

Indexed keywords

UBIQUITIN THIOLESTERASE;

ARTICLE; CONTROLLED STUDY; DISEASE PREDISPOSITION; EXON; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; ASIAN CONTINENTAL ANCESTRY GROUP; ETHNIC GROUPS; EXONS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; PARKINSON DISEASE; POLYMORPHISM, GENETIC; UBIQUITIN THIOLESTERASE;

EID: 54249162651     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (3)

1. Mcnaught KS, Jenner P. Proteasomal function is impaired in substantia nigra in Parkinson's disease. Neurosci Lett, 2001, 297:191-194.
2. von Bohlen und Halbach O, Schober A, Krieglstein K, et al. Genes, proteins, and neurotoxins involved in Parkinson's disease. Prog Neurobiol, 2004, 73:151-177.
3. Maraqanore DM, Lesnick TG, Elbaz A, et al. UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol, 2004, 55:512-521.