Spastin Binds to Lipid Droplets and Affects Lipid Metabolism

Mutations in SPAST, encoding spastin, are the most common cause of autosomal dominant hereditary spastic paraplegia (HSP). HSP is characterized by weakness and spasticity of the lower limbs, owing to progressive retrograde degeneration of the long corticospinal axons. Spastin is a conserved microtub...

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Detalles Bibliográficos
Autores principales: Papadopoulos, Chrisovalantis, Orso, Genny, Mancuso, Giuseppe, Herholz, Marija, Gumeni, Sentiljana, Tadepalle, Nimesha, Jüngst, Christian, Tzschichholz, Anne, Schauss, Astrid, Höning, Stefan, Trifunovic, Aleksandra, Daga, Andrea, Rugarli, Elena I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395272/
https://www.ncbi.nlm.nih.gov/pubmed/25875445
http://dx.doi.org/10.1371/journal.pgen.1005149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395272/
https://www.ncbi.nlm.nih.gov/pubmed/25875445
http://dx.doi.org/10.1371/journal.pgen.1005149

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