hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes

Published 2013 View Full Article

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Title
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
Authors
Keywords
-
Journal
NEUROBIOLOGY OF AGING
Volume 35, Issue 4, Pages 934.e5-934.e6
Publisher
Elsevier BV
Online
2013-10-09
DOI
10.1016/j.neurobiolaging.2013.09.016

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