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Schulte, E.C. et al.: Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease. Neurogenetics 13, 281-285 (2012)
* et al.: A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am. J. Hum. Genet. 89, 168-175 (2011)
Hartig, M.B. et al.: Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation. Am. J. Hum. Genet. 89, 543-550 (2011)
Hopfner, F. et al.: Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurology 11:134 (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)
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
Winkelmann, J. et al.: Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Mov. Disord. 23, 350-358 (2008)
García-Borreguero, D.* et al.: Diagnostic standards for dopaminergic augmentation of restless legs syndrome: Report from a World Association of Sleep Medicine-International Restless Legs Syndrome Study Group consensus conference at the Max Planck Institute. Sleep Med. 8, 520-530 (2007)
Kemlink, D. et al.: Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. Mov. Disord. 22, 207-212 (2007)
Winkelmann, J. et al.: Genetics of restless legs syndrome (RLS: State-of-the-art and future directions). Mov. Disord. 22, (Suppl.18), 449-458 (2007)
Winkelmann, J. et al.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)
Liebetanz, K.M.* et al.: RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. Neurology 67, 320-321 (2006)
Winkelmann, J. et al.: Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Mov. Disord. 21, 28-33 (2006)