Role of Common and Rare APP DNA Sequence Variants in Alzheimer Disease

Neurology - United States
doi 10.1212/wnl.0b013e3182515972
Full Text
Abstract

Available in full text

Categories
Neurology
Date
Authors
Publisher

Ovid Technologies (Wolters Kluwer Health)

Related search

Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

PLoS ONE
Multidisciplinary
2012English

The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci

Frontiers in Neurology
Neurology
2019English

Overlap Between Parkinson Disease and Alzheimer Disease inABCA7functional Variants

Neurology: Genetics
NeurologyGenetics
2016English

Common Mitochondrial Sequence Variants in Ischemic Stroke

Annals of Neurology
Neurology
2010English

Neural Phenotypes of Common and Rare Genetic Variants

Biological Psychology
NeurosciencePhysiological PsychologyNeuropsychology
2008English

Genetic Variants in Alzheimer Disease — Molecular and Brain Network Approaches

Nature Reviews Neurology
Molecular NeuroscienceNeurologyCellular
2016English

Association of Common and Rare Genetic Variants With Cognition in Schizophrenia

Canadian Journal of Biotechnology
2017English

DNA Sequence Variants and the Practice of Medicine

Current Opinion in Cardiology
Cardiovascular MedicineCardiology
2010English

The Role of APP in Alzheimer’s Disease

Advances in Alzheimer's Disease
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy