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, E.; Chartier, L.; Lam, R.; Da Barroca, S.; Moigneu, C.; Mairey, M.; Dussert, C.; Forlani, S.; Fontaine, B.; Seilhean, D.; Bohl, D.; Boillée, S.; Salachas, F.; Stevanin, G.; Millecamps, S.; Amador, M.-D.-M.; Meininger, V.; Lautrette, G.; Nicol, M.; Machat, S.; Couratier, P.; Larmonier, T.; Saker, S.
Source
In: Neurobiology of Aging . (Neurobiology of Aging, October 2017, 58:239.e11-239.e20)
Subject
Language
English
ISSN
15581497
01974580
01974580