Burden of genetic risk variants in multiple sclerosis families in the Netherlands

Background: Approximately 20% of multiple sclerosis patients have a family history of multiple sclerosis. Studies of multiple sclerosis aggregation in families are inconclusive. Objective: To investigate the genetic burden based on currently discovered genetic variants for multiple sclerosis risk in patients from Dutch multiple sclerosis multiplex families versus sporadic multiple sclerosis cases, and to study its influence on clinical phenotype and disease prediction. Methods: Our study population consisted of 283 sporadic multiple sclerosis cases, 169 probands from multiplex families and 202... Mehr ...

Verfasser: Mescheriakova, Julia Y.
Broer, Linda
Wahedi, Simin
Uitterlinden, André G.
van Duijn, Cornelia M.
Hintzen, Rogier Q.
Dokumenttyp: Artikel
Erscheinungsdatum: 2016
Reihe/Periodikum: Mescheriakova , J Y , Broer , L , Wahedi , S , Uitterlinden , A G , van Duijn , C M & Hintzen , R Q 2016 , ' Burden of genetic risk variants in multiple sclerosis families in the Netherlands ' , Multiple Sclerosis Journal - Experimental, Translational and Clinical , vol. 2 . https://doi.org/10.1177/2055217316648721
Schlagwörter: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being / name=SDG 3 - Good Health and Well-being
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29625299
Datenquelle: BASE; Originalkatalog
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Link(s) : https://pure.eur.nl/en/publications/0c3d8671-9237-4314-a27f-de16ec2100ed