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Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia. (2016)

First Author: Lynch DS

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/10.1001/jamaneurol.2016.2229

PubMed Identifier: 27749956

Publication URI: http://europepmc.org/abstract/MED/27749956

Type: Journal Article/Review

Volume: 73

Parent Publication: JAMA neurology

Issue: 12

ISSN: 2168-6149