bibliographic resource 1426565 [br/1426565]
https://w3id.org/oc/corpus/br/1426565

is a
title
  • hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
publication date
  • 2014-01-01
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