|
Volumn 67, Issue 3, 2010, Pages 414-415
|
Reply to: SNCA variants are associated with increased risk of multiple system atrophy
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ALPHA SYNUCLEIN;
ALLELE;
CASE CONTROL STUDY;
CONTROLLED STUDY;
GENE LOCUS;
GENETIC ASSOCIATION;
GENOME;
HUMAN;
LETTER;
MAJOR CLINICAL STUDY;
NEUROLOGIC DISEASE;
PARKINSON DISEASE;
PRIORITY JOURNAL;
RISK;
SHY DRAGER SYNDROME;
SINGLE NUCLEOTIDE POLYMORPHISM;
ALPHA-SYNUCLEIN;
BASE SEQUENCE;
BRAIN;
DNA MUTATIONAL ANALYSIS;
GENETIC MARKERS;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC TESTING;
GENETIC VARIATION;
HOMOZYGOTE;
HUMANS;
MULTIPLE SYSTEM ATROPHY;
ODDS RATIO;
POLYMORPHISM, SINGLE NUCLEOTIDE;
REGRESSION ANALYSIS;
REPRODUCIBILITY OF RESULTS;
RISK FACTORS;
|
EID: 77950532431
PISSN: 03645134
EISSN: 15318249
Source Type: Journal
DOI: 10.1002/ana.21786 Document Type: Letter |
Times cited : (34)
|
References (5)
|