|
Volumn 26, Issue 4, 2000, Pages 495-499
|
A point mutation in PTPRC is associated with the development of multiple sclerosis
a a a a a b b b c c d a b c a a |
Author keywords
[No Author keywords available]
|
Indexed keywords
PROTEIN TYROSINE PHOSPHATASE;
ADULT;
ARTICLE;
CONTROLLED STUDY;
EXON;
FEMALE;
GENE EXPRESSION;
GENE LOCUS;
HETEROZYGOSITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
MULTIPLE SCLEROSIS;
PHENOTYPE;
POINT MUTATION;
PRIORITY JOURNAL;
ANTIGENS, CD45;
BASE SEQUENCE;
CASE-CONTROL STUDIES;
DNA;
DNA PRIMERS;
EXONS;
FEMALE;
HETEROZYGOTE;
HUMANS;
MALE;
MULTIPLE SCLEROSIS;
PEDIGREE;
PHENOTYPE;
POINT MUTATION;
VARIATION (GENETICS);
|
EID: 0033662317
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/82659 Document Type: Article |
Times cited : (175)
|
References (26)
|