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

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@article{ee65e33e836442289baef9659d091bd0,

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

author = "T.H. Wong and A.J.M.H. Verkerk and A.J.M. Rozemuller and R. Willemsen and M. Neumann and V. Bonifati and {van Swieten}, J.C.",

year = "2015",

doi = "https://doi.org/10.1093/brain/awu333",

language = "English",

volume = "138",

journal = "Brain",

issn = "0006-8950",

publisher = "Oxford University Press",

}

TY - JOUR

T1 - Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease

AU - Wong, T.H.

AU - Verkerk, A.J.M.H.

AU - Rozemuller, A.J.M.

AU - Willemsen, R.

AU - Neumann, M.

AU - Bonifati, V.

AU - van Swieten, J.C.

PY - 2015

Y1 - 2015

U2 - https://doi.org/10.1093/brain/awu333

DO - https://doi.org/10.1093/brain/awu333

M3 - Article

C2 - 25414040

SN - 0006-8950

VL - 138

JO - Brain

JF - Brain

M1 - e358

ER -