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Spieler, D. et al.: Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon. Genome Res. 24, 592-603 (2014)
Wieczorek, D.* et al.: Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome. Am. J. Hum. Genet. 95, 698-707 (2014)
Zech, M. et al.: Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Mov. Disord. 29, 143-147 (2014)
Kaffe, M.: Functional analysis of the RLS-associated MEIS1 intronic locus. München, Technische Universität, Fakultät für Medizin, Diss., 2013, 106 S.
Kaffe, M. et al.: Mutational screening of THAP1 in a German population with primary dystonia. Parkinsonism Relat. Disord. 18, 104-106 (2012)
Schormair, B. et al.: MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease. J. Med. Genet. 48, 462-466 (2011)
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)