Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
Version of Record online: 21 MAY 2002
Copyright © 2002 Wiley-Liss, Inc.
Annals of Neurology
Volume 51, Issue 6, pages 794–795, June 2002
How to Cite
Muglia, M., Magariello, A., Nicoletti, G., Patitucci, A., Gabriele, A. L., Conforti, F. L., Mazzei, R., Caracciolo, M., Ardito, B., Lastilla, M., Tedeschi, G. and Quattrone, A. (2002), Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia. Ann Neurol., 51: 794–795. doi: 10.1002/ana.10185
- Issue online: 21 MAY 2002
- Version of Record online: 21 MAY 2002
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