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Amplifying the spectrum of SPAST gene mutations
Hereditary spastic paraplegias (HSPs) include a group of neurodegenerative disorders characterized by slowly progressive spasticity and weakness of the lower extremities, caused by axon degeneration of corticospinal tracts. Spastic paraplegia type 4 (SPG4) is the most common autosomal dominant form...
Autores principales: | Verriello, Lorenzo, Lonigro, Incoronata Renata, Pessa, Maria Elena, Betto, Elena, Pauletto, Giada, Fogolari, Federico, Gigli, Gian Luigi, Curcio, Francesco |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523053/ https://www.ncbi.nlm.nih.gov/pubmed/35132972 http://dx.doi.org/10.23750/abm.v92iS1.11608 |
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