C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. (2014)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000000061
PubMed Identifier: 24363131
Publication URI: http://europepmc.org/abstract/MED/24363131
Type: Journal Article/Review
Volume: 82
Parent Publication: Neurology
Issue: 4
ISSN: 0028-3878