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Correction: Solving unsolved rare neurological diseases—a S..:
Schüle, Rebecca
;
Timmann, Dagmar
;
Erasmus, Corrie E.
...
European Journal of Human Genetics. 29 (2021) 9 - p. 1462-1465 , 2021
Link:
https://doi.org/10.1038/s41431-021-00935-5
RT Journal T1
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41431-021-00935-5&Exemplar=1&LAN=DE A1 Schüle, Rebecca A1 Timmann, Dagmar A1 Erasmus, Corrie E. A1 Reichbauer, Jennifer A1 Wayand, Melanie A1 Baets, Jonathan A1 Balicza, Peter A1 Chinnery, Patrick A1 Dürr, Alexandra A1 Haack, Tobias A1 Hengel, Holger A1 Horvath, Rita A1 Houlden, Henry A1 Kamsteeg, Erik-Jan A1 Kamsteeg, Christoph A1 Lohmann, Katja A1 Macaya, Alfons A1 Marcé-Grau, Anna A1 Maver, Ales A1 Molnar, Judit A1 Münchau, Alexander A1 Peterlin, Borut A1 Riess, Olaf A1 Schöls, Ludger A1 Schüle, Rebecca A1 Stevanin, Giovanni A1 Synofzik, Matthis A1 Timmerman, Vincent A1 van de Warrenburg, Bart A1 van Os, Nienke PB Springer Science and Business Media LLC YR 2021 SN 1018-4813 SN 1476-5438 JF European Journal of Human Genetics VO 29 IS 9 SP 1462 OP 1465 LK http://dx.doi.org/https://doi.org/10.1038/s41431-021-00935-5 DO https://doi.org/10.1038/s41431-021-00935-5 SF ELIB - SuUB Bremen
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