PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease

Published 2014 View Full Article

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Title
PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease
Authors
Keywords
-
Journal
BRAIN
Volume 138, Issue 6, Pages e357-e357
Publisher
Oxford University Press (OUP)
Online
2014-11-21
DOI
10.1093/brain/awu332
References
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