Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice (2018)
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
Parent Publication: Human Molecular Genetics
Issue: 3
ISSN: 0964-6906