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Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells

For multiple sclerosis, genome wide association studies and follow up studies have identified susceptibility single nucleotide polymorphisms located in or near CLEC16A at chromosome 16p13.13, encompassing among others CIITA, DEXI and SOCS1 in addition to CLEC16A. These genetic variants are located i...

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發表在:PLoS One
Main Authors: Leikfoss, Ingvild S., Keshari, Pankaj K., Gustavsen, Marte W., Bjølgerud, Anja, Brorson, Ina S., Celius, Elisabeth G., Spurkland, Anne, Bos, Steffan D., Harbo, Hanne F., Berge, Tone
格式: Artigo
語言:Inglês
出版: Public Library of Science 2015
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4512731/
https://ncbi.nlm.nih.gov/pubmed/26203907
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0132957
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