Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency. (2014)

First Author: Melchionda L
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2014.08.003

PubMed Identifier: 25175347

Publication URI: http://europepmc.org/abstract/MED/25175347

Type: Journal Article/Review

Volume: 95

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297