Analysis of the stathmin rs182455 single nucleotide promoter polymorphism in patients with multiple sclerosis

Journal of Neurogenetics

Volumn 22, Issue 3, 2008, Pages 181-186

  Buttmann, Mathias ^a   Nowak, Eva ^a   Kroner, Antje ^a   Hemmer, Bernhard ^b   Lesch, Klaus Peter ^a   Rieckmann, Peter ^c  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Demyelination; Multiple sclerosis; Oligodendrocyte; Single nucleotide polymorphism; Stathmin

Indexed keywords

STATHMIN;

ARTICLE; CASE CONTROL STUDY; CHI SQUARE DISTRIBUTION; DISABILITY; FEMALE; GENE FREQUENCY; GENETICS; GENOTYPE; HUMAN; MALE; MULTIPLE SCLEROSIS; NUCLEOTIDE SEQUENCE; ONSET AGE; PROMOTER REGION; SINGLE STRAND CONFORMATION POLYMORPHISM;

AGE OF ONSET; CASE-CONTROL STUDIES; CHI-SQUARE DISTRIBUTION; DISABILITY EVALUATION; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; MALE; MULTIPLE SCLEROSIS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROMOTER REGIONS, GENETIC; STATHMIN;

EID: 76449092885     PISSN: 01677063     EISSN: 15635260     Source Type: Journal    
DOI: 10.1080/01677060802179287     Document Type: Article

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