Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases (original) (raw)

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11 Institute of Biochemistry I, Medical Faculty, University of Cologne, 50931 Cologne, Germany

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11 Institute of Biochemistry I, Medical Faculty, University of Cologne, 50931 Cologne, Germany

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11 Institute of Biochemistry I, Medical Faculty, University of Cologne, 50931 Cologne, Germany

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22 Department of Medicine III, University of Heidelberg, 69120 Heidelberg, Germany

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22 Department of Medicine III, University of Heidelberg, 69120 Heidelberg, Germany

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33 Department of Biology, Animal Physiology, University of Erlangen-Nuremberg, 91058 Erlangen, Germany

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11 Institute of Biochemistry I, Medical Faculty, University of Cologne, 50931 Cologne, Germany

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44 Department of Neurology, University Hospital Bonn, 53105 Bonn, Germany

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55 Institute of Neuropathology, University Hospital Erlangen, 91054 Erlangen, Germany

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66 Department of Biochemistry and Molecular Biology, University of Oviedo and University Institute of Biotechnology of Asturias, 33006 Oviedo, Spain

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Revision received:

07 June 2010

Published:

09 September 2010

Cite

Christoph S. Clemen, Karthikeyan Tangavelou, Karl-Heinz Strucksberg, Steffen Just, Linda Gaertner, Hanna Regus-Leidig, Maria Stumpf, Jens Reimann, Roland Coras, Reginald O. Morgan, Maria-Pilar Fernandez, Andreas Hofmann, Stefan Müller, Benedikt Schoser, Franz-Georg Hanisch, Wolfgang Rottbauer, Ingmar Blümcke, Stephan von Hörsten, Ludwig Eichinger, Rolf Schröder, Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases, Brain, Volume 133, Issue 10, October 2010, Pages 2920–2941, https://doi.org/10.1093/brain/awq222
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