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

2015-06-01

Brain: a journal of neurology , Volume 138 - Issue 6 p. e358

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Persistent URL	dx.doi.org/10.1093/brain/awu333, hdl.handle.net/1765/86104
Journal	Brain: a journal of neurology
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Wong, T.H, Verkerk, A, Rozemuller, A.J.M, Willemsen, R, Neumann, M, Bonifati, V, & van Swieten, J.C. (2015). Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease. Brain: a journal of neurology, 138(6). doi:10.1093/brain/awu333

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