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Neuroimaging features of C9ORF72 expansion
Published Web Location
http://europepmc.org/articles/PMC3580454?pdf=renderNo data is associated with this publication.
Abstract
Hexanucleotide expansion intronic to chromosome 9 open reading frame 72 (C9ORF72) has recently been identified as the most common genetic cause of both familial and sporadic amyotrophic lateral sclerosis and of frontotemporal dementia with or without conco
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