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


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 24161539

Publication URI:

Type: Journal Article/Review

Volume: 1842

Parent Publication: Biochimica et biophysica acta

Issue: 1

ISSN: 0006-3002