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Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease. (2019)

First Author: Ferrari Bardile C

Attributed to: How heterogeneous are oligodendroglia from normal human brain and spinal cord? funded by SPF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1073/pnas.1818042116

PubMed Identifier: 31015293

Publication URI: http://europepmc.org/abstract/MED/31015293

Type: Journal Article/Review

Volume: 116

Parent Publication: Proceedings of the National Academy of Sciences of the United States of America

Issue: 19

ISSN: 0027-8424