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Number of items: 2.
2018
Schormair, B.; Kemlink, D.; Mollenhauer, B.; Fiala, O.; Machetanz, G.; Roth, J.; Berutti, R.; Strom, T. M.; Haslinger, B.; Trenkwalder, C.; Zahorakova, D.; Martasek, P.; Ruzicka, E. and Winkelmann, J.
(2018):
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.
In: Clinical Genetics, Vol. 93, No. 3: pp. 603-612
2009
Kemlink, D.; Polo, O.; Frauscher, B.; Gschliesser, V.; Högl, B.; Meitinger, Thomas; Winkelmann, J.; Poewe, W.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S.; Schormair, B.; Lichtner, P.; Silander, K.; Peltonen, L.; Gieger, C.; Wichmann, Heinz-Erich; Zimprich, A.; Roeske, D. and Müller-Myhsok, B.
(2009):
Replication of restless legs syndrome loci in three European populations.
In: Journal of Medical Genetics, Vol. 46, No. 5: pp. 315-318
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