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

T.H. Wong, A.J.M.H. Verkerk, A.J.M. Rozemuller, R. Willemsen, M. Neumann, V. Bonifati, J.C. van Swieten

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Article numbere358
JournalBrain
Volume138
DOIs
Publication statusPublished - 2015

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