Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease. [electronic resource]
Producer: 20151109Description: 2881.e1-2881.e6 p. digitalISSN:- 1558-1497
- Aged
- Aged, 80 and over
- Alzheimer Disease -- diagnosis
- Amyloid beta-Protein Precursor -- genetics
- Cohort Studies
- Dementia -- diagnosis
- Diagnosis, Differential
- Female
- Genetic Association Studies
- Genetic Predisposition to Disease -- genetics
- Genetic Testing
- Genetic Variation -- genetics
- Humans
- Intercellular Signaling Peptides and Proteins -- genetics
- Male
- Middle Aged
- Presenilin-1 -- genetics
- Presenilin-2 -- genetics
- Prion Proteins
- Prions -- genetics
- Progranulins
- tau Proteins -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.