Publication
Title
PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease
Author
Language
English
Source (journal)
Brain. - London
Publication
Oxford : Oxford univ press , 2015
ISSN
0006-8950
DOI
10.1093/BRAIN/AWU332
Volume/pages
138 :6 (2015) , 2 p.
Article Reference
e357
ISI
000357999300005
Medium
E-only publicatie
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
External links
Web of Science
Record
Identifier
Creation 25.09.2019
Last edited 13.12.2024
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