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

Lookup NU author(s): Dr Ana TopfORCiD, Professor Volker StraubORCiD, Professor Chiara Marini Bettolo, Dr Sabine Specht

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Abstract

© 2021, The Author(s).In the original publication of the article, consortium author lists were missing in the article.


Publication metadata

Author(s): Schule R, Timmann D, Erasmus CE, Reichbauer J, Baets J, Chinnery P, Durr A, Haack T, Hengel H, Horvath R, Houlden H, Kamsteeg E-J, Kamsteeg C, Lohmann K, Macaya A, Maver A, Molnar J, Munchau A, Peterlin B, Riess O, Schols L, Schule R, Stevanin G, Synofzik M, Timmerman V, van de Warrenburg B, van Os N, Vandrovcova J, Wayand M, Wayand M, Wilke C, van de Warrenburg B, Schols L, Wilke C, Bevot A, Zuchner S, Beltran S, Laurie S, Synofzik M, Graessner H, Graessner H, Zurek B, Ellwanger K, Ossowski S, Demidov G, Sturm M, Schulze-Hentrich JM, Heutink P, Brunner H, Scheffer H, Hoogerbrugge N, Hoischen A, 't Hoen PAC, Vissers LELM, Gilissen C, Steyaert W, Sablauskas K, de Voer RM, Janssen E, de Boer E, Steehouwer M, Yaldiz B, Kleefstra T, Brookes AJ, Veal C, Gibson S, Wadsley M, Mehtarizadeh M, Riaz U, Warren G, Dizjikan FY, Shorter T, Topf A, Straub V, Marini Bettolo C, Specht S, Clayton-Smith J, Banka S, Alexander E, Jackson A, Faivre L, Thauvin C, Vitobello A, Denomme-Pichon A-S, Duffourd Y, Tisserant E, Bruel A-L, Peyron C, Pelissier A, Beltran S, Gut IG, Laurie S, Piscia D, Matalonga L, Matalonga L, Papakonstantinou A, Bullich G, Corvo A, Garcia C, Fernandez-Callejo M, Hernandez C, Pico D, Paramonov I, Lochmuller H, Gumus G, Bros-Facer V, Rath A, Hanauer M, Olry A, Lagorce D, Havrylenko S, Izem K, Rigour F, Durr A, Davoine C-S, Guillot-Noel L, Heinzmann A, Coarelli G, Bonne G, Evangelista T, Allamand V, Nelson I, Yaou RB, Metay C, Eymard B, Cohen E, Atalaia A, Stojkovic T, Macek M, Turnovec M, Thomasova D, Kremlikova RP, Frankova V, Havlovicova M, Kremlik V, Parkinson H, Keane T, Spalding D, Senf A, Robinson P, Danis D, Robert G, Costa A, Patch C, Hanna M, Houlden H, Reilly M, Vandrovcova J, Muntoni F, Zaharieva I, Sarkozy A, de Jonghe P, Nigro V, Banfi S, Torella A, Musacchia F, Piluso G, Ferlini A, Selvatici R, Rossi R, Neri M, Aretz S, Spier I, Sommer AK, Peters S, Oliveira C, Pelaez JG, Matos AR, Jose CS, Ferreira M, Gullo I, Fernandes S, Garrido L, Ferreira P, Carneiro F, Swertz MA, Johansson L, van der Velde JK, van der Vries G, Neerincx PB, Roelofs-Prins D, Kohler S, Metcalfe A, Verloes A, Drunat S, Rooryck C, Trimouille A, Castello R, Morleo M, Pinelli M, Varavallo A, De la Paz MP, Sanchez EB, Martin EL, Delgado BM, de la Rosa FJAG, Ciolfi A, Dallapiccola B, Pizzi S, Radio FC, Tartaglia M, Renieri A, Benetti E, Balicza P, Balicza P, Molnar MJ, Maver A, Peterlin B, Munchau A, Lohmann K, Herzog R, Pauly M, Macaya A, Marce-Grau A, Marce-Grau A, Osorio AN, de Benito DN, Lochmuller H, Thompson R, Polavarapu K, Beeson D, Cossins J, Cruz PMR, Hackman P, Johari M, Savarese M, Udd B, Horvath R, Capella G, Valle L, Holinski-Feder E, Laner A, Steinke-Lange V, Schrock E, Rump A

Publication type: Note

Publication status: Published

Journal: European Journal of Human Genetics

Year: 2021

Volume: 29

Pages: 1462–1465

Print publication date: 01/09/2021

Online publication date: 25/08/2021

Acceptance date: 02/04/2020

ISSN (print): 1018-4813

ISSN (electronic): 1476-5438

Publisher: Springer Nature

URL: https://doi.org/10.1038/s41431-021-00935-5

DOI: 10.1038/s41431-021-00935-5


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