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Volumn 120, Issue 1-2, 2001, Pages 138-145

Genetic variation in the transforming growth factor β1 gene in multiple sclerosis

(7) Weinshenker, Brian G a Hebrink, David a Kantarci, Orhun H a Schaefer Klein, Janet a Atkinson, Elizabeth a Schaid, Daniel a McMurray, Cynthia M a

a MAYO CLINIC (United States)

Author keywords

Multiple sclerosis; Neurogenetics; Neuroimmunology; Transforming growth factor 1

Indexed keywords

DNA; TRANSFORMING GROWTH FACTOR BETA1;

ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE PREDISPOSITION; DNA FINGERPRINTING; DNA POLYMORPHISM; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HAPLOTYPE; HETEROZYGOTE DETECTION; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MULTIPLE SCLEROSIS; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL;

ADULT; CHROMOSOMES, HUMAN, PAIR 19; EXONS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; MULTIPLE SCLEROSIS; MUTATION, MISSENSE; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS); TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA1; VARIATION (GENETICS);

EID: 0034750527 PISSN: 01655728 EISSN: None Source Type: Journal
DOI: 10.1016/S0165-5728(01)00424-6 Document Type: Article

Times cited : (21)

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