Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and 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.bbadis.2013.10.008
PubMed Identifier: 24161539
Publication URI: http://europepmc.org/abstract/MED/24161539
Type: Journal Article/Review
Parent Publication: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Issue: 1
ISSN: 0006-3002