CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature. (2023)
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/10.1093/hmg/ddad161
PubMed Identifier: 37815936
Publication URI: http://europepmc.org/abstract/MED/37815936
Type: Journal Article/Review
Volume: 33
Parent Publication: Human molecular genetics
Issue: 1
ISSN: 0964-6906