APA

Martin E., Schüle R., Smets K., Rastetter A., Boukhris A., Loureiro J. L., Gonzalez M. A., Mundwiller E., Deconinck T., Wessner M., Jornea L., Oteyza A. C., Durr A., Martin J., Schöls L., Mhiri C., Lamari F., Züchner S., De Jonghe P., Kabashi E., Brice A. & Stevanin G. (20130404). Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. : American journal of human genetics.

Chicago

Martin Elodie, Schüle Rebecca, Smets Katrien, Rastetter Agnès, Boukhris Amir, Loureiro José L, Gonzalez Michael A, Mundwiller Emeline, Deconinck Tine, Wessner Marc, Jornea Ludmila, Oteyza Andrés Caballero, Durr Alexandra, Martin Jean-Jacques, Schöls Ludger, Mhiri Chokri, Lamari Foudil, Züchner Stephan, De Jonghe Peter, Kabashi Edor, Brice Alexis and Stevanin Giovanni. 20130404. Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. : American journal of human genetics.

Harvard

Martin E., Schüle R., Smets K., Rastetter A., Boukhris A., Loureiro J. L., Gonzalez M. A., Mundwiller E., Deconinck T., Wessner M., Jornea L., Oteyza A. C., Durr A., Martin J., Schöls L., Mhiri C., Lamari F., Züchner S., De Jonghe P., Kabashi E., Brice A. and Stevanin G. (20130404). Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. : American journal of human genetics.

MLA

Martin Elodie, Schüle Rebecca, Smets Katrien, Rastetter Agnès, Boukhris Amir, Loureiro José L, Gonzalez Michael A, Mundwiller Emeline, Deconinck Tine, Wessner Marc, Jornea Ludmila, Oteyza Andrés Caballero, Durr Alexandra, Martin Jean-Jacques, Schöls Ludger, Mhiri Chokri, Lamari Foudil, Züchner Stephan, De Jonghe Peter, Kabashi Edor, Brice Alexis and Stevanin Giovanni. Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. : American journal of human genetics. 20130404.