M - 10 Mutations du gène NIPA1 (SPG6) : une cause rare de...

Revue Neurologique 2007 / 4 Vol. 163; Iss. 4

M - 10 Mutations du gène NIPA1 (SPG6) : une cause rare de paraparésie spastique héréditaire en Europe

Klebe, S., Lacour, A., Durr, A., Stojkovic, T., Depienne, C., Forlani, S., Poca-Guyon, S., Vuillaume, I., Sablonniere, B., Vermersch, P., Brice, A., Stevanin, G.
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Volume:
163
Language:
french
Journal:
Revue Neurologique
DOI:
10.1016/S0035-3787(07)90706-7
Date:
April, 2007
File:
PDF, 56 KB
french, 2007
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