Rare variants in the CYP27B1 gene are associated with multiple sclerosis

Annals of Neurology

Volumn 70, Issue 6, 2011, Pages 881-886

  Ramagopalan, Sreeram V ^a,b   Dyment, David A ^c   Cader, M Zameel ^b,d   Morrison, Katie M ^a,b   Disanto, Giulio ^a,b   Morahan, Julia M ^a,b   Berlanga Taylor, Antonio J ^a,b   Handel, Adam ^a,b   De Luca, Gabriele C ^a,b   Sadovnick, A Dessa ^e   Lepage, Pierre ^f   Montpetit, Alexandre ^f   Ebers, George C ^a,b  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c UNIVERSITY OF OTTAWA   (Canada)

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^f MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CALCITRIOL; CYP27B1 PROTEIN; CYTOCHROME P450; UNCLASSIFIED DRUG; VITAMIN D DEPENDENT RICKETS I PROTEIN;

ADULT; ARTICLE; CONTROLLED STUDY; EXOME; EXOME SEQUENCING; FEMALE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HUMAN; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MALE; MULTIPLE SCLEROSIS; PARENT; PREVALENCE; PRIORITY JOURNAL; PROGENY; SINGLE NUCLEOTIDE POLYMORPHISM;

25-HYDROXYVITAMIN D3 1-ALPHA-HYDROXYLASE; AGE OF ONSET; COHORT STUDIES; EXOME; FAMILY HEALTH; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MULTIPLE SCLEROSIS; MUTATION; VITAMIN D DEFICIENCY;

EID: 84255175933     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22678     Document Type: Article

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