Novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family. (2013)

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/10.1016/j.neurobiolaging.2013.06.005

PubMed Identifier: 23870839

Publication URI: http://europepmc.org/abstract/MED/23870839

Type: Journal Article/Review

Volume: 34

Parent Publication: Neurobiology of aging

Issue: 12

ISSN: 0197-4580