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	doi.org/10.1093/brain/awu333, hdl.handle.net/1765/86104
Journal	Brain: a journal of neurology
Organisation	Department of Internal Medicine
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Wong, T. H., Verkerk, A., Rozemuller, A., Willemsen, R., Neumann, M., Bonifati, V., & van Swieten, J. (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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