Winkelmann, J., P. Lichtner, B. Schormair, M. Uhr, S. Hauk, K. Stiasny-Kolster, C. Trenkwalder, W. Paulus, I. Peclau, I. Eisensehr, T. Illig, H. E. Wichmann, H. Pfister, J. Golic, T. Bettecken, B. Pütz, F. Holsboer, T. Meitinger and B. Müller-Myhsok: Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. In: Movement Disorders 23, 3, 350-358 (2008).
Winkelmann, J., B. Schormair, P. Lichtner, S. Ripke, L. Xiong, S. Jalilzadeh, S. Fulda, B. Pütz, G. Eckstein, S. Hauk, C. Trenkwalder, A. Zimprich, K. Stiasny-Kolster, W. Oertel, C. G. Bachmann, W. Paulus, I. Peglau, I. Eisensehr, J. Montplaisir, G. Turecki, G. Rouleau, C. Gieger, T. Illig, E. Wichmann, F. Holsboer, B. Müller-Myhsok and T. Meitinger: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. In: Nature Genetics 39, 8, 1000-1006 (2007).
Winkelmann, J., P. Lichtner, B. Pütz, C. Trenkwalder, S. Hauk, T. Meitinger, T. Strom and B. Müller-Myhsok: Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. In: Movement Disorders 21, 1, 28-33 (2006).
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.