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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications
Tim W. Rattay, Tobias Lindig, Jonathan Baets, Katrien Smets, Tine Deconinck, Anne S. Söhn, Konstanze Hörtnagel, Kathrin N. Eckstein, Sarah Wiethoff, Jennifer Reichbauer, Marion Döbler-Neumann, Ingeborg Krägeloh-Mann, Michaela Auer-Grumbach, Barbara Plecko, Alexander Münchau, Bernd Wilken, Marc Janauschek, Anne Katrin Giese, Jan L. De Bleecker, Els Ortibus
- University of Tubingen
- German Centre for Neurodegenerative Diseases (DZNE)
- University of Antwerp
- University of Vienna
- Zurich Center for Integrative Human Physiology (ZIHP)
- Klinikum Kassel
- University of Greifswald
- Kinderhospital Osnabrück
- Harvard University
- Ghent University
- KU Leuven
- Centro de Investigación Biomedica en Red de Enfermedades Neurodegenerativas (CIBERNED)
- Universidad del País Vasco (UPV/EHU)
- Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Raras, CIBERER
- Catalan Institution for Research and Advanced Studies
- IRCCS Istituto Eugenio Medea - Bosisio Parini (LC)
- John P. Hussman Institute for Human Genomics
- University of Miami
- Dr. John T. Macdonald Foundation
- Centogene AG