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...

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Detalles Bibliográficos
Autores principales: Verriello, Lorenzo, Lonigro, Incoronata Renata, Pessa, Maria Elena, Betto, Elena, Pauletto, Giada, Fogolari, Federico, Gigli, Gian Luigi, Curcio, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2021
Materias:
Case Report
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

Internet

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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