Homozygous TREM2 mutation in a family with atypical frontotemporal dementia. (2014)
Attributed to:
A systematic investigation into the pathogenesis and course of Parkinson's syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2014.04.010
PubMed Identifier: 24910390
Publication URI: http://europepmc.org/abstract/MED/24910390
Type: Journal Article/Review
Volume: 35
Parent Publication: Neurobiology of aging
Issue: 10
ISSN: 0197-4580