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

✍ Scribed by Roberto Del Bo; Alessio Di Fonzo; Serena Ghezzi; Federica Locatelli; Giovanni Stevanin; Antonella Costa; Stefania Corti; Nereo Bresolin; Giacomo Pietro Comi

Publisher: Springer
Year: 2007
Tongue: English
Weight: 257 KB
Volume: 8
Category: Article
ISSN: 1364-6745
DOI: 10.1007/s10048-007-0095-z

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