4.5 Article

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

Journal

NEUROBIOLOGY OF AGING
Volume 35, Issue 4, Pages 934.e5-934.e6

Publisher

Elsevier BV
DOI: 10.1016/j.neurobiolaging.2013.09.016

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