The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
- Author(s):
- Bladen, C.L.; Salgado, D.; Monges, S.; Foncuberta, M.E.; Kekou, K.; Kosma, K.; Dawkins, H.; Lamont, L.; Roy, A.J.; Chamova, T.; Guergueltcheva, V.; Chan, S.; Korngut, L.; Campbell, C.; Dai, Y.; Wang, J.; Barisic, N.; Brabec, P.; Lahdetie, J.; Walter, M.C.; Schreiber-Katz, O.; Karcagi, V.; Garami, M.; Viswanathan, V.; Bayat, F.; Buccella, F.; Kimura, E.; Koeks, Z.; Bergen, J.C. van den; Rodrigues, M.; Roxburgh, R.; Lusakowska, A.; Kostera-Pruszczyk, A.; Zimowski, J.; Santos, R.; Neagu, E.; Artemieva, S.; Rasic, V.M.; Vojinovic, D.; Posada, M.; Bloetzer, C.; Jeannet, P.Y.; Joncourt, F.; Diaz-Manera, J.; Gallardo, E.; Karaduman, A.A.; Topaloglu, H.; Sherif, R. el; Stringer, A.; Shatillo, A.V.; Martin, A.S.; Peay, H.L.; Bellgard, M.I.; Kirschner, J.; Flanigan, K.M.; Straub, V.; Bushby, K.; Verschuuren, J.; Aartsma-Rus, A.; Beroud, C.; Lochmuller, H.
- Published
- 2015
- Publication type
- Article / Letter to editor
DMDDuchenne muscular dystrophyTREAT-NMDrare disease registries
- Date issued
- 2015-04-30
- Language
- English
- Is part of
- Human Mutation (2015), Vol. 36, no. 4, p. 395-402
- hdl
- 1887/107191
- doi
- 10.1002/humu.22758