TY  - JOUR
AU  - Gil-Varea, Elia
AU  - Fedetz, Maria
AU  - Eixarch, Herena
AU  - Spataro, Nino
AU  - Villar, Luisa Maria
AU  - Urcelay, Elena
AU  - Saiz, Albert
AU  - Fernandez, Oscar
AU  - Leyva, Laura
AU  - Ramio-Torrenta, Lluis
AU  - Vandenbroeck, Koen
AU  - Otaegui, David
AU  - Castillo-Triviño, Tamara
AU  - Izquierdo, Guillermo
AU  - Malhotra, Sunny
AU  - Bosch, Elena
AU  - Navarro, Arcadi
AU  - Alcina, Antonio
AU  - Montalban, Xavier
AU  - Matesanz, Fuencisla
AU  - Comabella, Manuel
PY  - 2020
DO  - 10.3390/jcm9030625
SN  - 2077-0383
UR  - https://hdl.handle.net/10668/26956
T2  - Journal of clinical medicine
AB  - Genome-wide association studies and meta-analysis have contributed to the identification of more than 200 loci associated with multiple sclerosis (MS). However, a proportion of MS heritability remains unknown. We aimed to uncover new genetic variants...
LA  - en
PB  - MDPI
KW  - CXCR5
KW  - Genetics
KW  - Genotyping
KW  - Multiple sclerosis
KW  - Single nucleotide polymorphisms
KW  - Targeted DNA sequencing
KW  - Alleles
KW  - T-Lymphocytes, Regulatory
KW  - Peptide Elongation Factors
KW  - Linkage Disequilibrium
KW  - Immunophenotyping
TI  - A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells.
TY  - research article
VL  - 9
ER  -