%0 Journal Article %J American Journal of Human Genetics %D 2014 %T Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia %A Esteves, T. %A Durr, A. %A Mundwiller, E. %A Loureiro, J.L. %A Boutry, M. %A Gonzalez, M. A. %A Gauthier, J. %A El-Hachimi, K.H. %A Depienne, C. %A Muriel, M.-P. %A Acosta Lebrigio, R.F. %A Gaussen, M. %A Noreau, A. %A Speziani, F. %A Dionne-Laporte, A. %A Deleuze, J.-F. %A Dion, P. %A Coutinho, P. %A Rouleau, G.A. %A Zuchner, S. %A Brice, A. %A Stevanin, G. %A Darios, F. %B American Journal of Human Genetics %V 94 %P 268 - 277 %8 2014 %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-84893774987&partnerID=40&md5=f46b0f13ecd79dfff83bab02179218f3 %N 2 %0 Journal Article %J American Journal of Human Genetics %D 2013 %T Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia %A Martin, E. %A Schüle, R. %A Smets, K. %A Rastetter, A. %A Boukhris, A. %A Loureiro, J.L. %A Gonzalez, M. A. %A Mundwiller, E. %A Deconinck, T. %A Wessner, M. %A Jornea, L. %A Oteyza, A. C. %A Durr, A. %A Martin, J. -J. %A Schöls, L. %A Mhiri, C. %A Lamari, F. %A Züchner, S. %A De Jonghe, P. %A Kabashi, E. %A Brice, A. %A Stevanin, G. %B American Journal of Human Genetics %V 92 %P 238 - 244 %8 2013/// %G eng %U http://www.scopus.com/inward/record.url?eid=2-s2.0-84873707921&partnerID=40&md5=a7c36595271f81fa0773d0c5d0689ca2 %N 2