Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation. (2016)

First Author: Spiegel R


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2015-103361

PubMed Identifier: 26561570

Publication URI: http://europepmc.org/abstract/MED/26561570

Type: Journal Article/Review

Volume: 53

Parent Publication: Journal of medical genetics

Issue: 2

ISSN: 0022-2593