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Browsing by Author Koppers, M.
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2012 | VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient | van Blitterswijk, M.; Van Es, M.A.; Koppers, M.; van Rheenen, W.; Medic, J., et al |
| 2012 | UNC13A is a modifier of survival in amyotrophic lateral sclerosis. | Diekstra, F.P.; Vught, P.W. van; Rheenen, W. van; Koppers, M.; Pasterkamp, R.J., et al |
| 2012 | VCP mutations in familial and sporadic amyotrophic lateral sclerosis. | Koppers, M.; Blitterswijk, M.M. van; Vlam, L.; Rowicka, P.A.; Vught, P.W. van, et al |
| 2011 | Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. | Es, M.A. van; Schelhaas, H.J.; Vught, P.W. van; Ticozzi, N.; Andersen, P.M., et al |
| 2010 | A large genome scan for rare CNVs in amyotrophic lateral sclerosis. | Blauw, H.M.; Al-Chalabi, A.; Andersen, P.M.; Vught, P.W. van; Diekstra, F.P., et al |
Showing results 1 to 5 of 5
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