Association of α-synuclein gene haplotypes with Parkinson's disease

Parkinsonism and Related Disorders

Volumn 13, Issue 6, 2007, Pages 343-347

  Parsian, A J ^a   Racette, B A ^b   Zhao, J H ^c   Sinha, R ^a   Patra, B ^a   Perlmutter, J S ^b   Parsian, A ^a  

^a ARKANSAS CHILDREN S HOSPITAL RESEARCH INSTITUTE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

synuclein; Haplotype; Parkinson; Single nucleotide polymorphism (SNP)

Indexed keywords

ALPHA SYNUCLEIN;

ADULT; AFRICAN AMERICAN; AGED; ALLELE; AMERICAN INDIAN; ARTICLE; CONTROLLED STUDY; DINUCLEOTIDE REPEAT; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; ALPHA-SYNUCLEIN; DINUCLEOTIDE REPEATS; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; PARKINSON DISEASE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 34547770262     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2006.12.006     Document Type: Article

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