MAPT p.V363I mutation: A rare cause of corticobasal degeneration. (2019)
Attributed to:
Investigation of the genetic and functional determinants of disease progression in Progressive Supranuclear Palsy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000347
PubMed Identifier: 31404212
Publication URI: http://europepmc.org/abstract/MED/31404212
Type: Journal Article/Review
Volume: 5
Parent Publication: Neurology. Genetics
Issue: 4
ISSN: 2376-7839