Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis. [electronic resource]
- Journal of medical genetics Jan 2013
- 25-33 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1468-6244
10.1136/jmedgenet-2012-101085 doi
25-Hydroxyvitamin D3 1-alpha-Hydroxylase--genetics Chromosome Mapping Chromosomes, Human, Pair 12 Enhancer Elements, Genetic Genetic Predisposition to Disease Genome-Wide Association Study Humans Kinesins--genetics Methyltransferases--genetics Multiple Sclerosis--genetics Polymorphism, Single Nucleotide Quantitative Trait Loci Transcription, Genetic