Mutation of the Human Mitochondrial Phenylalanine-Trna Synthetase Causes Infantile-Onset Epilepsy and Cytochrome C Oxidase Deficiency

AuthID
 P-008-GVK
12
Author(s)
Almalki, A
·
Alston, CL
·
Parker, A
·
Simonic, I
·
Mehta, SG
·
He, LP
·
Reza, M
·
McFarland, R
·
Document Type
Article
Year published
2014
Published
in BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, ISSN: 0925-4439
Volume: 1842, Issue: 1, Pages: 56-64 (9)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 24161539
Scopus: 2-s2.0-84887641296
Wos: WOS:000332500800006
Source Identifiers
ISSN: 0925-4439
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