학술논문
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis
Document Type
Article
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
Source
In Neurobiology of Aging October 2017 58:239-239
Subject
Language
ISSN
0197-4580