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 Molnar; Alexander 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

doi:10.1038/s41431-021-00935-5

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 Molnar

Alexander 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 › Academic

Abstract

In the original publication of the article, consortium author lists were missing in the article.

Original language	English
Pages (from-to)	1462-1465
Number of pages	4
Journal	European Journal of Human Genetics
Volume	29
Issue number	9
DOIs	https://doi.org/10.1038/s41431-021-00935-5
Publication status	Published - 1 Sept 2021

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10.1038/s41431-021-00935-5

1 Editorial

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

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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., ... SOLVE-RD Consortium (2021). Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint. European Journal of Human Genetics, 29(9), 1462-1465. https://doi.org/10.1038/s41431-021-00935-5

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title = "Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint",

abstract = "In the original publication of the article, consortium author lists were missing in the article.",

author = "Rebecca Sch{\"u}le and Dagmar Timmann and Erasmus, \{Corrie E.\} and Jennifer Reichbauer and Melanie Wayand and Jonathan Baets and Peter Balicza and Patrick Chinnery and Alexandra D{\"u}rr and Tobias Haack and Holger Hengel and Rita Horvath and Henry Houlden and Kamsteeg, \{Erik Jan\} and Christoph Kamsteeg and Katja Lohmann and Alfons Macaya and Anna Marc{\'e}-Grau and Ales Maver and Judit Molnar and Alexander M{\"u}nchau and Borut Peterlin and Olaf Riess and Ludger Sch{\"o}ls and Giovanni Stevanin and Matthis Synofzik and Vincent Timmerman and \{van de Warrenburg\}, Bart and \{van Os\}, Nienke and Jana Vandrovcova and Carlo Wilke and Andrea Bevot and Stephan Zuchner and Sergi Beltran and Steven Laurie and Leslie Matalonga and Holm Graessner and Birte Zurek and Kornelia Ellwanger and Stephan Ossowski and German Demidov and Marc Sturm and Han Brunner and Solve-RD-DITF-RND and \{SOLVE-RD Consortium\}",

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doi = "10.1038/s41431-021-00935-5",

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Schüle, R, Timmann, D, Erasmus, CE, Reichbauer, J, Wayand, M, Baets, J, Balicza, P, Chinnery, P, Dürr, A, Haack, T, Hengel, H, Horvath, R, Houlden, H, Kamsteeg, EJ, Kamsteeg, C, Lohmann, K, Macaya, A, Marcé-Grau, A, Maver, A, Molnar, J, Münchau, 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 2021, 'Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint', European Journal of Human Genetics, vol. 29, no. 9, pp. 1462-1465. https://doi.org/10.1038/s41431-021-00935-5

TY - JOUR

T1 - Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint

AU - Schüle, Rebecca

AU - Timmann, Dagmar

AU - Erasmus, Corrie E.

AU - Reichbauer, Jennifer

AU - Wayand, Melanie

AU - Baets, Jonathan

AU - Balicza, Peter

AU - Chinnery, Patrick

AU - Dürr, Alexandra

AU - Haack, Tobias

AU - Hengel, Holger

AU - Horvath, Rita

AU - Houlden, Henry

AU - Kamsteeg, Erik Jan

AU - Kamsteeg, Christoph

AU - Lohmann, Katja

AU - Macaya, Alfons

AU - Marcé-Grau, Anna

AU - Maver, Ales

AU - Molnar, Judit

AU - Münchau, Alexander

AU - Peterlin, Borut

AU - Riess, Olaf

AU - Schöls, Ludger

AU - Stevanin, Giovanni

AU - Synofzik, Matthis

AU - Timmerman, Vincent

AU - van de Warrenburg, Bart

AU - van Os, Nienke

AU - Vandrovcova, Jana

AU - Wilke, Carlo

AU - Bevot, Andrea

AU - Zuchner, Stephan

AU - Beltran, Sergi

AU - Laurie, Steven

AU - Matalonga, Leslie

AU - Graessner, Holm

AU - Zurek, Birte

AU - Ellwanger, Kornelia

AU - Ossowski, Stephan

AU - Demidov, German

AU - Sturm, Marc

AU - Brunner, Han

AU - Solve-RD-DITF-RND

AU - SOLVE-RD Consortium

PY - 2021/9/1

Y1 - 2021/9/1

N2 - In the original publication of the article, consortium author lists were missing in the article.

AB - In the original publication of the article, consortium author lists were missing in the article.

U2 - 10.1038/s41431-021-00935-5

DO - 10.1038/s41431-021-00935-5

M3 - Erratum / corrigendum

SN - 1018-4813

VL - 29

SP - 1462

EP - 1465

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -

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

Abstract

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Research output

Solving unsolved rare neurological diseases-a Solve-RD viewpoint

Cite this