Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement (2012)

First Author: Guerreiro R
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/10.1001/archneurol.2013.579

Publication URI: http://dx.doi.org/10.1001/archneurol.2013.579

Type: Journal Article/Review

Parent Publication: JAMA Neurology