학술논문
Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy
Document Type
Article
Author
Haack, T.B.; Iuso, A.; Kremer, L.S.; Hartig, M.; Strom, T.M.; Meitinger, T.; Prokisch, H.; Gorza, M.; Graf, E.; Berutti, R.; Ignatius, E.; Isohanni, P.; Suomalainen, A.; Carroll, C.J.; Lönnqvist, T.; Calvo-Garrido, J.; Stranneheim, H.; Wedell, A.; Maffezzini, C.; Freyer, C.; Wredenberg, A.; Paucar, M.; Svenningsson, P.; Brandberg, G.; Kurian, M.A.; Hayflick, S.A.; Hayflick, S.A.; Venco, P.; Tiranti, V.; Dichgans, M.; Klopstock, T.; Horvath, R.; Holinski-Feder, E.; Senderek, J.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 1 September 2016, 99(3):735-743)
Subject
Language
English
ISSN
15376605
00029297
00029297