Solving unsolved rare neurological diseases-a Solve-RD viewpoint

Rebecca Schuele*, Dagmar Timmann, Corrie E. Erasmus, Jennifer Reichbauer, Melanie Wayand, Bart van de Warrenburg, Ludger Schoels, Carlo Wilke, Andrea Bevot, Stephan Zuchner, Sergi Beltran, Steven Laurie, Leslie Matalonga, Holm Graessner, Matthis Synofzik, Solve-RD-DITF-RND, SOLVE-RD Consortium, Han Brunner

*Corresponding author for this work

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  • 2021

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

    Schüle, R., Timmann, D., Erasmus, C. E., Reichbauer, J., Wayand, M., Baets, J., Balicza, P., Chinnery, P., Dürr, A., Haack, T., Hengel, H., Horvath, R., Houlden, H., Kamsteeg, E. J., Kamsteeg, C., Lohmann, K., Macaya, A., Marcé-Grau, A., Maver, A., Molnar, J., & 25 othersMünchau, A., Peterlin, B., Riess, O., Schöls, L., Stevanin, G., Synofzik, M., Timmerman, V., van de Warrenburg, B., van Os, N., Vandrovcova, J., Wilke, C., Bevot, A., Zuchner, S., Beltran, S., Laurie, S., Matalonga, L., Graessner, H., Zurek, B., Ellwanger, K., Ossowski, S., Demidov, G., Sturm, M., Brunner, H., Solve-RD-DITF-RND & SOLVE-RD Consortium, 1 Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1462-1465 4 p.

    Research output: Contribution to journalErratum / corrigendum / retractionsAcademic

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