APA

Klebe S., Lacour A., Durr A., Stojkovic T., Depienne C., Forlani S., Poea-Guyon S., Vuillaume I., Sablonniere B., Vermersch P., Brice A. & Stevanin G. (20080123). NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. : Neurogenetics.

Chicago

Klebe Stephan, Lacour Arnaud, Durr Alexandra, Stojkovic Tanya, Depienne Christel, Forlani Sylvie, Poea-Guyon Sandrine, Vuillaume Isabelle, Sablonniere Bernard, Vermersch Patrick, Brice Alexis and Stevanin Giovanni. 20080123. NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. : Neurogenetics.

Harvard

Klebe S., Lacour A., Durr A., Stojkovic T., Depienne C., Forlani S., Poea-Guyon S., Vuillaume I., Sablonniere B., Vermersch P., Brice A. and Stevanin G. (20080123). NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. : Neurogenetics.

MLA

Klebe Stephan, Lacour Arnaud, Durr Alexandra, Stojkovic Tanya, Depienne Christel, Forlani Sylvie, Poea-Guyon Sandrine, Vuillaume Isabelle, Sablonniere Bernard, Vermersch Patrick, Brice Alexis and Stevanin Giovanni. NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe. : Neurogenetics. 20080123.