Publication
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
C. Beetz, R. Schule, T. Deconinck, K.-N. Tran-Viet, H. Zhu, B. P.H. Kremer, S. G.M. Frints, W. A.G. van Zelst-Stams, P. Byrne, S. Otto, A. O.H. Nygren, J. Baets, K. Smets, B. Ceulemans, B. Dan, N. Nagan, J. Kassubek, S. Klimpe, T. Klopstock, H. Stolze, H. J.M. Smeets, C. T.R.M. Schrander-Stumpel, M. Hutchinson, B. P. van de Warrenburg, C. Braastad, T. Deufel, M. Pericak-Vance, L. Schols, P. de Jonghe, S. Zuchner
Brain, February 2008, Oxford University Press (OUP)
DOI: 10.1093/brain/awn026