Expanding the phenotype of de novo SLC25A4 -linked mitochondrial disease to include mild myopathy (2018)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000256
Publication URI: http://dx.doi.org/10.1212/nxg.0000000000000256
Type: Journal Article/Review
Parent Publication: Neurology Genetics
Issue: 4