REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.
par Beetz, Christian;Schüle, Rebecca;Deconinck, Tine;Tran-Viet, Khanh-Nhat;Zhu, Hui;Kremer, B;Frints, Suzanna G M;van Zelst-Stams, Wendy A G;Byrne, Paula;Otto, Susanne;Nygren, Anders O H;Baets, Jonathan;Smets, Katrien;Ceulemans, Berten;Dan, Bernard 
;Nagan, Narasimhan;Kassubek, Jan;Klimpe, Sven;Klopstock, Thomas;Stolze, Henning;Smeets, Hubert J M;Schrander-Stumpel, Constance T R M;Hutchinson, Michael;van de Warrenburg, B P;Braastad, Corey;Deufel, Thomas;Pericak-Vance, M A;Schöls, Lüdger;de Jonghe, Peter;Züchner, Stephan
Référence Brain, 131, Pt 4, page (1078-1086)
Publication Publié, 2008-04
;Nagan, Narasimhan;Kassubek, Jan;Klimpe, Sven;Klopstock, Thomas;Stolze, Henning;Smeets, Hubert J M;Schrander-Stumpel, Constance T R M;Hutchinson, Michael;van de Warrenburg, B P;Braastad, Corey;Deufel, Thomas;Pericak-Vance, M A;Schöls, Lüdger;de Jonghe, Peter;Züchner, StephanRéférence Brain, 131, Pt 4, page (1078-1086)
Publication Publié, 2008-04
Article révisé par les pairs
