Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease. (2019)

First Author: Oláhová M

Attributed to: Centre for Ageing and Vitality funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddz202

PubMed Identifier: 31435670

Publication URI: http://europepmc.org/abstract/MED/31435670

Type: Journal Article/Review

Volume: 28

Parent Publication: Human molecular genetics

Issue: 22

ISSN: 0964-6906