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Volumn 248, Issue 9, 2001, Pages 979-984
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No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
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Author keywords
Association; Genetic; Parkinson's disease; Polymorphism; UCH L1
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Indexed keywords
GENE PRODUCT;
HYDROLASE;
UBIQUITIN;
UBIQUITIN CARBOXY TERMINAL HYDROLASE L1;
UNCLASSIFIED DRUG;
THIOL ESTER HYDROLASE;
UBIQUITIN THIOLESTERASE;
ADULT;
AGED;
ALLELE;
ARTICLE;
CARBOXY TERMINAL SEQUENCE;
CODON;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
DISEASE PREDISPOSITION;
DNA POLYMORPHISM;
ETHNIC DIFFERENCE;
EXON;
FAMILIAL DISEASE;
FEMALE;
GENE FREQUENCY;
GENETIC ASSOCIATION;
GENETIC RISK;
GENETIC SUSCEPTIBILITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PARKINSON DISEASE;
POPULATION RESEARCH;
PRIORITY JOURNAL;
ENZYMOLOGY;
FRANCE;
GENETIC POLYMORPHISM;
GENETIC SCREENING;
GENETICS;
GENOTYPE;
METABOLISM;
MIDDLE AGED;
MUTATION;
NUCLEOTIDE SEQUENCE;
ONSET AGE;
PATHOPHYSIOLOGY;
SEX DIFFERENCE;
AGE OF ONSET;
AGED;
DNA MUTATIONAL ANALYSIS;
FEMALE;
FRANCE;
GENE FREQUENCY;
GENETIC SCREENING;
GENOTYPE;
HUMANS;
MALE;
MIDDLE AGED;
MUTATION;
PARKINSON DISEASE;
POLYMORPHISM, GENETIC;
SEX FACTORS;
THIOLESTER HYDROLASES;
UBIQUITIN THIOLESTERASE;
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EID: 0034864346
PISSN: 03405354
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (42)
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References (16)
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