Additional Metadata
Persistent URL dx.doi.org/10.1093/brain/awu333, hdl.handle.net/1765/86104
Journal Brain: a journal of neurology
Citation
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