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About this Medicine article
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis by Teyssou, Elisa; Chartier, Laura; Amador, Maria-Del-Mar; Lam, Roselina; Lautrette, Géraldine; Nicol, Marie; Machat, Selma; Da Barroca, Sandra; Moigneu, Carine; Mairey, Mathilde; Larmonier, Thierry; Saker, Safaa; Dussert, Christelle; Forlani, Sylvie; Fontaine, Bertrand; Seilhean, Danielle; Bohl, Delphine; Boillée, Séverine; Meininger, Vincent; Couratier, Philippe; Salachas, François; Stevanin, Giovanni; Millecamps, Stéphanie is a Medicine article available to read on EtoBox.
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- Author
- Teyssou, Elisa; Chartier, Laura; Amador, Maria-Del-Mar; Lam, Roselina; Lautrette, Géraldine; Nicol, Marie; Machat, Selma; Da Barroca, Sandra; Moigneu, Carine; Mairey, Mathilde; Larmonier, Thierry; Saker, Safaa; Dussert, Christelle; Forlani, Sylvie; Fontaine, Bertrand; Seilhean, Danielle; Bohl, Delphine; Boillée, Séverine; Meininger, Vincent; Couratier, Philippe; Salachas, François; Stevanin, Giovanni; Millecamps, Stéphanie
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0197-4580)
- Published
- 2017
- Field
- Medicine (Health Sciences)