SPG11: a consistent clinical phenotype in a family with...

SPG11: a consistent clinical phenotype in a family with homozygous Spatacsin truncating mutation

Roberto Del Bo, Alessio Di Fonzo, Serena Ghezzi, Federica Locatelli, Giovanni Stevanin, Antonella Costa, Stefania Corti, Nereo Bresolin, Giacomo Pietro Comi
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Volume:
8
Language:
english
Pages:
5
DOI:
10.1007/s10048-007-0095-z
Date:
November, 2007
File:
PDF, 257 KB
english, 2007
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