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Genome Research|March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonDerek Spieler, Maria Kaffe, Franziska Knauf, et al.The Lancet. Neurology|October 15, 2017
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysisBarbara Schormair, Chen Zhao, Steven Bell, et al.Brain : a Journal of Neurology|February 12, 2025
Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystoniaMichael Zech, Ivana Dzinovic, Matej Skorvanek, et al.Pageof 2