Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene

Background: Hereditary spastic paraparesis (HSP) denotes a group of inherited neurological disorders with progressive lower limb spasticity as their clinical hallmark; a large proportion of autosomal dominant HSP belongs to HSP type 4, which has been linked to the SPG4 locus on chromosome 2. A varie...

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Main Authors: Bonsch, D, Schwindt, A, Navratil, P, Palm, D, Neumann, C, Klimpe, S, Schickel, J, Hazan, J, Weiller, C, Deufel, T, Liepert, J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2003
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Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1738610/
https://ncbi.nlm.nih.gov/pubmed/12876245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.74.8.1109
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