> Details
Schüle, Rebecca;
Timmann, Dagmar;
Erasmus, Corrie E.;
Reichbauer, Jennifer;
Wayand, Melanie;
Baets, Jonathan;
Balicza, Peter;
Chinnery, Patrick;
Dürr, Alexandra;
Haack, Tobias;
Hengel, Holger;
Horvath, Rita;
Houlden, Henry;
Kamsteeg, Erik-Jan;
Kamsteeg, Christoph;
Lohmann, Katja;
Macaya, Alfons;
Marcé-Grau, Anna;
Maver, Ales;
Molnar, Judit;
Münchau, Alexander;
Peterlin, Borut;
Riess, Olaf;
Schöls, Ludger;
[...]
Solving unsolved rare neurological diseases—a Solve-RD viewpoint
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- Media type: E-Article
- Title: Solving unsolved rare neurological diseases—a Solve-RD viewpoint
- Contributor: Schüle, Rebecca; Timmann, Dagmar; Erasmus, Corrie E.; Reichbauer, Jennifer; Wayand, Melanie; Baets, Jonathan; Balicza, Peter; Chinnery, Patrick; Dürr, Alexandra; Haack, Tobias; Hengel, Holger; Horvath, Rita; Houlden, Henry; Kamsteeg, Erik-Jan; Kamsteeg, Christoph; Lohmann, Katja; Macaya, Alfons; Marcé-Grau, Anna; Maver, Ales; Molnar, Judit; Münchau, Alexander; Peterlin, Borut; Riess, Olaf; Schöls, Ludger; [...]
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Published:
Springer Science and Business Media LLC, 2021
- Published in: European Journal of Human Genetics, 29 (2021) 9, Seite 1332-1336
- Language: English
- DOI: 10.1038/s41431-021-00901-1
- ISSN: 1018-4813; 1476-5438
- Origination:
- Footnote:
- Access State: Open Access