NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe
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author: Patrick Vermersch Alexandra Durr Sylvie Forlani Sandrine Poea-Guyon Giovanni Stevanin Bernard Sablonniere Christel Depienne Isabelle Vuillaume Alexis Brice Stephan Klebe Tanya Stojkovic Arnaud Lacour |
| Publication date | January 5, 2007 |
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