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Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis |
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Titel: |
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis |
Auteur: |
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 |
Verschenen in: |
Neurobiology of aging |
Paginering: |
Jaargang 58 (2017) nr. C pagina's 239.e11-239.e20 |
Jaar: |
2017 |
Inhoud: |
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Uitgever: |
Elsevier Inc. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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