Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Solve-RD-DITF-RND; The Solve-RD Consortium; Rebecca Schüle; Dagmar Timmann; Corrie E. Erasmus; Jennifer Reichbauer; Melanie Wayand; Jonathan Baets; Peter Balicza; Patrick Chinnery; Alexandra Durr; Tobias Haack; Holger Hengel; Rita Horvath; Henry Houlden; Erik Jan Kamsteeg; Christoph Kamsteeg; Katja Lohmann; Alfons Macaya; Anna Marcé-Grau; Ales Maver; Maria Judit Molnar; Alexander Münchau; Borut Peterlin; Olaf Riess; Ludger Schöls; Rebecca Schüle; Giovanni Stevanin; Matthis Synofzik; Vincent Timmerman; Bart van de Warrenburg; Nienke van Os; Jana Vandrovcova; Melanie Wayand; Carlo Wilke; Bart van de Warrenburg; Ludger Schöls; Carlo Wilke; Andrea Bevot; Stephan Zuchner; Sergi Beltran; Steven Laurie; Leslie Matalonga; Holm Graessner; Matthis Synofzik; Holm Graessner; Birte Zurek; Kornelia Ellwanger; Alexander Münchau; Katja Lohmann; Rebecca Herzog; Martje Pauly

doi:10.1038/s41431-021-00935-5

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

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

^*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

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

Originalsprache	Englisch
Zeitschrift	European Journal of Human Genetics
Jahrgang	29
Ausgabenummer	9
Seiten (von - bis)	1462-1465
Seitenumfang	4
ISSN	1018-4813
DOIs	https://doi.org/10.1038/s41431-021-00935-5
Publikationsstatus	Veröffentlicht - 09.2021

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen
SDG 10 – Weniger Ungleichheiten

Strategische Forschungsbereiche und Zentren

Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

DFG-Fachsystematik

2.23-07 Klinische Neurologie, Neurochirurgie und Neuroradiologie

Dokumente

10.1038/s41431-021-00935-5

Weitere Links

Link to publication in Scopus

Zitieren

Solve-RD-DITF-RND, The Solve-RD Consortium, Schüle, R., Timmann, D., Erasmus, C. E., Reichbauer, J., Wayand, M., Baets, J., Balicza, P., Chinnery, P., Durr, A., Haack, T., Hengel, H., Horvath, R., Houlden, H., Kamsteeg, E. J., Kamsteeg, C., Lohmann, K., Macaya, A., ... Pauly, M. (2021). Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1). 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 (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)",

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

author = "Solve-RD-DITF-RND and \{The Solve-RD Consortium\} and 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 Durr 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 Molnar, \{Maria Judit\} and Alexander M{\"u}nchau and Borut Peterlin and Olaf Riess and Ludger Sch{\"o}ls and Rebecca Sch{\"u}le and Giovanni Stevanin and Matthis Synofzik and Vincent Timmerman and \{van de Warrenburg\}, Bart and \{van Os\}, Nienke and Jana Vandrovcova and Melanie Wayand and Carlo Wilke and \{van de Warrenburg\}, Bart and Ludger Sch{\"o}ls and Carlo Wilke and Andrea Bevot and Stephan Zuchner and Sergi Beltran and Steven Laurie and Leslie Matalonga and Holm Graessner and Matthis Synofzik and Holm Graessner and Birte Zurek and Kornelia Ellwanger and Alexander M{\"u}nchau and Katja Lohmann and Rebecca Herzog and Martje Pauly",

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year = "2021",

month = sep,

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Solve-RD-DITF-RND, The Solve-RD Consortium, Schüle, R, Timmann, D, Erasmus, CE, Reichbauer, J, Wayand, M, Baets, J, Balicza, P, Chinnery, P, Durr, A, Haack, T, Hengel, H, Horvath, R, Houlden, H, Kamsteeg, EJ, Kamsteeg, C, Lohmann, K, Macaya, A, Marcé-Grau, A, Maver, A, Molnar, MJ, Münchau, A, Peterlin, B, Riess, O, Schöls, L, Schüle, R, Stevanin, G, Synofzik, M, Timmerman, V, van de Warrenburg, B, van Os, N, Vandrovcova, J, Wayand, M, Wilke, C, van de Warrenburg, B, Schöls, L, Wilke, C, Bevot, A, Zuchner, S, Beltran, S, Laurie, S, Matalonga, L, Graessner, H, Synofzik, M, Graessner, H, Zurek, B, Ellwanger, K, Münchau, A , Lohmann, K , Herzog, R & Pauly, M 2021, 'Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)', European Journal of Human Genetics, Jg. 29, Nr. 9, S. 1462-1465. https://doi.org/10.1038/s41431-021-00935-5

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1). / Solve-RD-DITF-RND; The Solve-RD Consortium; Schüle, Rebecca et al.
in: European Journal of Human Genetics, Jahrgang 29, Nr. 9, 09.2021, S. 1462-1465.

Publikation: Beiträge in Fachzeitschriften › Kommentare/Debatten

TY - JOUR

T1 - Correction

T2 - Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

AU - Solve-RD-DITF-RND

AU - The Solve-RD Consortium

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 - Durr, 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, Maria Judit

AU - Münchau, Alexander

AU - Peterlin, Borut

AU - Riess, Olaf

AU - Schöls, Ludger

AU - Schüle, Rebecca

AU - Stevanin, Giovanni

AU - Synofzik, Matthis

AU - Timmerman, Vincent

AU - van de Warrenburg, Bart

AU - van Os, Nienke

AU - Vandrovcova, Jana

AU - Wayand, Melanie

AU - Wilke, Carlo

AU - van de Warrenburg, Bart

AU - Schöls, Ludger

AU - Wilke, Carlo

AU - Bevot, Andrea

AU - Zuchner, Stephan

AU - Beltran, Sergi

AU - Laurie, Steven

AU - Matalonga, Leslie

AU - Graessner, Holm

AU - Synofzik, Matthis

AU - Graessner, Holm

AU - Zurek, Birte

AU - Ellwanger, Kornelia

AU - Münchau, Alexander

AU - Lohmann, Katja

AU - Herzog, Rebecca

AU - Pauly, Martje

PY - 2021/9

Y1 - 2021/9

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.

UR - https://www.scopus.com/pages/publications/85114607324

U2 - 10.1038/s41431-021-00935-5

DO - 10.1038/s41431-021-00935-5

M3 - Comments/Debates

C2 - 34429526

AN - SCOPUS:85114607324

SN - 1018-4813

VL - 29

SP - 1462

EP - 1465

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -