| Authors: |
Kretz A; Department of Neurology, Jena University Hospital, 07747 Jena, Germany. Electronic address: alexandra.kretz@med.uni-jena.de., Arbeiter M; Neurological Clinic Fürth, 90766 Fürth, Germany., Strobel J; Department of Transfusion Medicine and Hemostaseology, University Hospital Erlangen, 91054 Erlangen, Germany., Blum K; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany., Frischholz B; Department of Transfusion Medicine and Hemostaseology, University Hospital Erlangen, 91054 Erlangen, Germany., Rödiger A; Department of Neurology, Jena University Hospital, 07747 Jena, Germany; Centre for Rare Diseases (ZSE), Jena University Hospital, 07747 Jena, Germany., Hackstein H; Department of Transfusion Medicine and Hemostaseology, University Hospital Erlangen, 91054 Erlangen, Germany., Maihöfner C; Neurological Clinic Fürth, 90766 Fürth, Germany., Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany; Centre for Rare Diseases Erlangen (ZSEER), Universitätsklinikum Erlangen, 91054 Erlangen, Germany., Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany; Centre for Rare Diseases Erlangen (ZSEER), Universitätsklinikum Erlangen, 91054 Erlangen, Germany., Schwab M; Department of Neurology, Jena University Hospital, 07747 Jena, Germany. |
