MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy. (2019)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddz093
PubMed Identifier: 31039582
Publication URI: http://europepmc.org/abstract/MED/31039582
Type: Journal Article/Review
Volume: 28
Parent Publication: Human molecular genetics
Issue: 16
ISSN: 0964-6906