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Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. (2019)

First Author: Saoura M

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