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Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. (2014)

First Author: Almalki A
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

Volume: 1842

Parent Publication: Biochimica et biophysica acta

Issue: 1

ISSN: 0006-3002