A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation

Marina Scarlato; Arturo Nuara; Simonetta Gerevini; Sara Benedetti; Paolo Rossi; Maurizio Ferrari; Stefano Carlo Previtali

doi:10.1007/s00415-014-7606-2

A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation

Marina Scarlato, Arturo Nuara, Simonetta Gerevini, Sara Benedetti, Paolo Rossi, Maurizio Ferrari, Stefano Carlo Previtali

IRCCS Ospedale San Raffaele

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	476-478
Number of pages	3
Journal	Journal of Neurology
Volume	262
Issue number	2
DOIs	https://doi.org/10.1007/s00415-014-7606-2
Publication status	Published - 2014

ASJC Scopus subject areas

Clinical Neurology
Neurology
Medicine(all)

Access to Document

10.1007/s00415-014-7606-2

Cite this

A new double-trouble phenotype : fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. / Scarlato, Marina; Nuara, Arturo; Gerevini, Simonetta ; Benedetti, Sara; Rossi, Paolo; Ferrari, Maurizio ; Previtali, Stefano Carlo.

In: Journal of Neurology, Vol. 262, No. 2, 2014, p. 476-478.

Research output: Contribution to journal › Article › peer-review

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author = "Marina Scarlato and Arturo Nuara and Simonetta Gerevini and Sara Benedetti and Paolo Rossi and Maurizio Ferrari and Previtali, {Stefano Carlo}",

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AU - Ferrari, Maurizio

AU - Previtali, Stefano Carlo

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