Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy

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Author(s)Haack TB, Ignatius E, Calvo-Garrido J, Iuso A, Isohanni P, Maffezzini C, Lonnqvist T, Suomalainen A, Gorza M, Kremer LS, Graf E, Hartig M, Berutti R, Paucar M, Svenningsson P, Stranneheim H, Brandberg G, Wedell A, Kurian MA, Hayflick SA, Venco P, Tiranti V, Strom TM, Dichgans M, Horvath R, Holinski-Feder E, Freyer C, Meitinger T, Prokisch H, Senderek J, Wredenberg A, Carroll CJ, Klopstock T
Publication type Article
JournalAmerican Journal of Human Genetics
Year2016
Volume99
Issue3
Pages735-743
ISSN (print)0002-9297
ISSN (electronic)1537-6605
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PublisherCell Press
URLhttp://dx.doi.org/10.1016/j.ajhg.2016.06.026
DOI10.1016/j.ajhg.2016.06.026
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