A New Risk Variant for Multiple Sclerosis at 11q23.3
CXCR5
genetics
genotyping
multiple sclerosis
single nucleotide polymorphisms
targeted DNA sequencing
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
26 Feb 2020
26 Feb 2020
Historique:
received:
16
01
2020
revised:
19
02
2020
accepted:
20
02
2020
entrez:
1
3
2020
pubmed:
1
3
2020
medline:
1
3
2020
Statut:
epublish
Résumé
Genome-wide association studies and meta-analysis have contributed to the identification of more than 200
Identifiants
pubmed: 32110891
pii: jcm9030625
doi: 10.3390/jcm9030625
pmc: PMC7141122
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : ISCIII-SGEFI/FEDER
ID : PT13/0001
Organisme : AEI/FEDER
ID : BFU2016-77961-P
Organisme : MINECO
ID : MDM-2014-0370
Organisme : Instituto de Salud Carlos III
ID : PI12/02229, PI15/00587, PI16/01259
Organisme : Red Española de Esclerosis Múltiple
ID : RD16/0015/0004, RD16/0015/0002; RD16/0015/0016
Organisme : Ministerio de Economía, Industria y Competitividad
ID : SAF2016-80595-C2-1-P
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