Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation
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Title
Symmetrical Corticobasal Syndrome Caused by a Novel c.314dup Progranulin Mutation
Authors
Keywords
-
Journal
JOURNAL OF MOLECULAR NEUROSCIENCE
Volume 45, Issue 3, Pages 354-358
Publisher
Springer Nature
Online
2011-08-24
DOI
10.1007/s12031-011-9626-z
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Note: Only part of the references are listed.- TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia
- (2010) J. D. Rohrer et al. NEUROLOGY
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- (2006) Luisa Benussi et al. NEUROBIOLOGY OF AGING
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