Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease. (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.2014.06.002
PubMed Identifier: 25104557
Publication URI: http://europepmc.org/abstract/MED/25104557
Type: Journal Article/Review
Volume: 35
Parent Publication: Neurobiology of aging
Issue: 12
ISSN: 0197-4580