Professur für Humangenetik
Präsidium der Justus-Liebig-Universität Gießen » Fachbereiche » Fachbereich 11 - Humanmedizin » Dekanat Fachbereich 11 - Humanmedizin » Zentrum für Klinische Chemie, Klinische Immunologie und Humangenetik
Type of organisation: Professorship
Publications 
2 of 2 
2 of 2
- Codon 101 of PRKCG, a preferential mutation site in SCA14 (2007)
Nolte, Dagmar; Klebe, Stephan; Mueller, Ulrich - Nigrostriatal dysfunction in X-linked dystonia-parkinsonism (DYT3) (2007)
Tackenberg, Bjoern; Metz, Aline; Unger, Marcus; et al. - Spinocerebellar ataxia 14:: Novel mutation in exon 2 of PRKCG in a German family (2007)
Nolte, Dagmar; Landendinger, Melanie; Schmitt, Eberhard; et al. - Structural and functional analysis of the human TAF1/DYT3 multiple transcript system (2007)
Herzfeld, Thilo; Nolte, Dagmar; Mueller, Ulrich - Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor - A unusual clinical benefit (2007)
Freund, Hans-Joachim; Barnikol, Utako B.; Nolte, Dagmar; et al. - The TAF1/DYT3 multiple transcript system in X-linked dystonia-parkinsonism (2007)
Mueller, Ulrich; Herzfeld, Thilo; Nolte, Dagmar - Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes (2006)
Waters, MF; Minassian, NA; Stevanin, G; et al. - Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2) (2006)
Tuin, I.; Voss, U.; Kang, J.-S.; et al. - An autosomal dominant ataxia maps to 19q13:: Allelic heterogeneity of SCA13 or novel locus? (2005)
Waters, MF; Fee, D; Figueroa, KP; et al.
