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

Author

Marina Scarlato

Sara Benedetti

Stefano C. Previtali

Paolo Rossi

Published in: Journal of Neurology

Date of publication: December 16, 2014

Main subject: paraparesis, Fascioscapulohumeral Muscular Dystrophy, spastic paraparesis

Bibliographic databases:

Cites articles 10

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Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype
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Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype

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