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

Brain

1 Department of Neurology, Erasmus Medical Centre, 3015 CE Rotterdam, The Netherlands 7 Alzheimer Centre, Neuroscience Campus Amsterdam, 1007 MB Amsterdam, The Netherlands 8 Department of Neurology, Neuroscience Campus Amsterdam, 1007 MB Amsterdam, The Netherlands

Published: June 2015

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614125PMC
http://dx.doi.org/10.1093/brain/awu333DOI Listing

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