Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint

Rebecca Schüle^*, Dagmar Timmann, Corrie E. Erasmus, Jennifer Reichbauer, Melanie Wayand, Jonathan Baets, Peter Balicza, Patrick Chinnery, Alexandra Dürr, Tobias Haack, Holger Hengel, Rita Horvath, Henry Houlden, Erik Jan Kamsteeg, Christoph Kamsteeg, Katja Lohmann, Alfons Macaya, Anna Marcé-Grau, Ales Maver, Judit MolnarAlexander Münchau, Borut Peterlin, Olaf Riess, Ludger Schöls, Giovanni Stevanin, Matthis Synofzik, Vincent Timmerman, Bart van de Warrenburg, Nienke van Os, Jana Vandrovcova, Carlo Wilke, Andrea Bevot, Stephan Zuchner, Sergi Beltran, Steven Laurie, Leslie Matalonga, Holm Graessner, Birte Zurek, Kornelia Ellwanger, Stephan Ossowski, German Demidov, Marc Sturm, Han Brunner, Solve-RD-DITF-RND, SOLVE-RD Consortium

^*Corresponding author for this work

Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

1 Editorial

1 results

Filter

2021

Solving unsolved rare neurological diseases-a Solve-RD viewpoint
Schuele, R., Timmann, D., Erasmus, C. E., Reichbauer, J., Wayand, M., van de Warrenburg, B., Schoels, L., Wilke, C., Bevot, A., Zuchner, S., Beltran, S., Laurie, S., Matalonga, L., Graessner, H., Synofzik, M., Solve-RD-DITF-RND, SOLVE-RD Consortium & Brunner, H., Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1332-1336 5 p.
Research output: Contribution to journal › Editorial › Academic › peer-review

Open Access

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint

Research output

Search results

Solving unsolved rare neurological diseases-a Solve-RD viewpoint