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Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)
Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, Matthis Synofzik, Dagmar Timmann, Tine Holemans, Albena Andreeva, Jennifer Reichbauer, Riet De Rycke, Dae In Chang, Sarah Van Veen, Jean Samuel, Ludger Schöls, Thorsten Pöppel, Danny Mollerup Sørensen, Bob Asselbergh, Christine Klein, Stephan Zuchner, Albena Jordanova*, Peter Vangheluwe
*Corresponding author for this work
- Molecular Neurogenomics Group
- University of Antwerp
- KU Leuven
- Department of Neurology
- University of Sofia
- University of Tubingen
- German Centre for Neurodegenerative Diseases (DZNE)
- Department of Neurology
- University of Duisburg-Essen
- Inflammation Research Center
- Ghent University
- Department of Nuclear Medicine
- University of Miami
- Molecular Medicine Center
- Department of Cognitive Science and Psychology
- New Bulgarian University
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