A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders. (2019)
Attributed to:
The UK GENetic Frontotemporal dementia Initiative (UK GENFI)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/mcs.a003913
PubMed Identifier: 31160356
Publication URI: http://europepmc.org/abstract/MED/31160356
Type: Journal Article/Review
Volume: 5
Parent Publication: Cold Spring Harbor molecular case studies
Issue: 3
ISSN: 2373-2873