@article{
 title = {EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders},
 type = {article},
 year = {2024},
 pages = {66},
 volume = {19},
 month = {2},
 day = {14},
 id = {7e27c972-de4e-3fd7-b5ee-54a65fc38219},
 created = {2025-01-16T14:10:50.604Z},
 file_attached = {false},
 profile_id = {17c87d5d-2470-32d7-b273-0734a1d9195f},
 last_modified = {2025-01-16T14:27:27.676Z},
 read = {false},
 starred = {false},
 authored = {true},
 confirmed = {false},
 hidden = {false},
 private_publication = {false},
 bibtype = {article},
 author = {Atalaia, Antonio and Wandrei, Dagmar and Lalout, Nawel and Thompson, Rachel and Tassoni, Adrian and ’t Hoen, Peter A. C. and Athanasiou, Dimitrios and Baker, Suzie-Ann and Sakellariou, Paraskevi and Paliouras, Georgios and D’Angelo, Carla and Horvath, Rita and Mancuso, Michelangelo and van der Beek, Nadine and Kornblum, Cornelia and Kirschner, Janbernd and Pareyson, Davide and Bassez, Guillaume and Blacas, Laura and Jacoupy, Maxime and Eng, Catherine and Lamy, François and Plançon, Jean-Philippe and Haberlova, Jana and Brusse, Esther and Hoeijmakers, Janneke G. J. and de Visser, Marianne and Claeys, Kristl G. and Paradas, Carmen and Toscano, Antonio and Silani, Vincenzo and Gyenge, Melinda and Reviers, Evy and Hamroun, Dalil and Vroom, Elisabeth and Wilkinson, Mark D. and Lochmuller, Hanns and Evangelista, Teresinha},
 doi = {10.1186/s13023-024-03059-3},
 journal = {Orphanet Journal of Rare Diseases},
 number = {1}
}

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