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Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy. (2016)

First Author: Haack TB

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2016.06.026

PubMed Identifier: 27545679

Publication URI: http://europepmc.org/abstract/MED/27545679

Type: Journal Article/Review

Volume: 99

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297