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Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease. (2012)

First Author: Guerreiro RJ

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.2011.10.009

PubMed Identifier: 22153900

Publication URI: http://europepmc.org/abstract/MED/22153900

Type: Journal Article/Review

Volume: 33

Parent Publication: Neurobiology of aging

Issue: 5

ISSN: 0197-4580