Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. (2019)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.23777
PubMed Identifier: 31045291
Publication URI: http://europepmc.org/abstract/MED/31045291
Type: Journal Article/Review
Volume: 40
Parent Publication: Human mutation
Issue: 10
ISSN: 1059-7794