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Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice. (2018)

First Author: So E

Attributed to: Exome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variants funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddx415

PubMed Identifier: 29194538

Publication URI: http://europepmc.org/abstract/MED/29194538

Type: Journal Article/Review

Volume: 27

Parent Publication: Human molecular genetics

Issue: 3

ISSN: 0964-6906