MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy. (2019)

First Author: Bugiardini E

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