RRM1 variants cause a mitochondrial DNA maintenance disorder via impaired de novo nucleotide synthesis. (2022)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1172/jci145660
PubMed Identifier: 35617047
Publication URI: http://europepmc.org/abstract/MED/35617047
Type: Journal Article/Review
Volume: 132
Parent Publication: The Journal of clinical investigation
Issue: 13
ISSN: 0021-9738