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TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT. (2013)

First Author: Ling H

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.011

PubMed Identifier: 23664753

Publication URI: http://europepmc.org/abstract/MED/23664753

Type: Journal Article/Review

Volume: 34

Parent Publication: Neurobiology of aging

Issue: 12

ISSN: 0197-4580