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