REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

Christian Beetz, Rebecca Schüle, Tine Deconinck, Khanh Nhat Tran-Viet, Hui Zhu, Berry P.H. Kremer, Suzanna G.M. Frints, Wendy A.G. Van Zelst-Stams, Paula Byrne, Susanne Otto, Anders O.H. Nygren, Jonathan Baets, Katrien Smets, Berten Ceulemans, Bernard Dan, Narasimhan Nagan, Jan Kassubek, Sven Klimpe, Thomas Klopstock, Henning StolzeHubert J.M. Smeets, Constance T.R.M. Schrander-Stumpel, Michael Hutchinson, Bart P. Van De Warrenburg, Corey Braastad, Thomas Deufel, Margaret Pericak-Vance, Ludger Schöls, Peter De Jonghe, Stephan Züchner

Research output: Contribution to journalArticlepeer-review

130 Scopus citations

Fingerprint

Dive into the research topics of 'REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31'. Together they form a unique fingerprint.

Medicine & Life Sciences