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Movement Disorders Clinical Practice|October 27, 2018
Iron in Restless Legs SyndromeEva C Schulte, Maria Kaffe, Barbara Schormair, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2013
Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controlsMichael Zech, Nadine Gross, Angela Jochim, et al.Journal of Medical Genetics|May 17, 2011
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal diseaseBarbara Schormair, Jens Plag, Maria Kaffe, et al.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.American Journal of Human Genetics|December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.Plos Genetics|July 23, 2011
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1Juliane Winkelmann, Darina Czamara, Barbara Schormair, et al.Pageof 1