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Article

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

Journal of neurology - 1 Feb 2015

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

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Share to Adenosine Triphosphatases
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscular Dystrophy, Facioscapulohumeral

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Share to Spastic Paraplegia, Hereditary

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Source

Identifiers

PMID: 25511172
DOI: 10.1007/s00415-014-7606-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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