Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy (2016)
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
Parent Publication: The American Journal of Human Genetics
Issue: 3