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

Research output: Contribution to journal › Letter › peer-review

Access to Document

@article{22fcc2ea7f52484bb150f25921a32bc0,

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

author = "Cyril Pottier and Matt Baker and Dickson, \{Dennis W.\} and Rosa Rademakers",

year = "2015",

month = jun,

day = "1",

doi = "10.1093/brain/awu332",

language = "English",

volume = "138",

pages = "e357",

journal = "Brain",

issn = "0006-8950",

number = "6",

}

TY - JOUR

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

AU - Pottier, Cyril

AU - Baker, Matt

AU - Dickson, Dennis W.

AU - Rademakers, Rosa

PY - 2015/6/1

Y1 - 2015/6/1

UR - https://www.scopus.com/pages/publications/84937511679

U2 - 10.1093/brain/awu332

DO - 10.1093/brain/awu332

M3 - Letter

C2 - 25414037

AN - SCOPUS:84937511679

SN - 0006-8950

VL - 138

SP - e357

JO - Brain

JF - Brain

IS - 6

ER -