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

Cyril Pottier, Matt Baker, Dennis W. Dickson, Rosa Rademakers

Research output: Contribution to journalLetter

5 Scopus citations
Original languageEnglish (US)
Pages (from-to)e357
JournalBrain
Volume138
Issue number6
DOIs
StatePublished - Jun 1 2015

ASJC Scopus subject areas

  • Clinical Neurology

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