SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
Year: 2009
Type: article
Study design: Observational Study
Source: Neurology
Authors: C. Goizet, A. Boukhris, D. Maltete, L. Guyant-Maréchal, J. Truchetto, E. Mundwiller, S. Hanein, P. Jonveaux, F. Roelens, J. Loureiro, E. Godet, S. Forlani, J. Melki, M. Auer-Grumbach, J. C. Fernandez, P. Martin-Hardy, I. Sibon, G. Sole, I. Orignac, C. Mhiri, P. Coutinho, A. Durr, A. Brice, G. Stevanin
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2013371339