Author:
Takezawa Yusuke,Fujie Hiromi,Kikuchi Atsuo,Niihori Tetsuya,Funayama Ryo,Shirota Matsuyuki,Nakayama Keiko,Aoki Yoko,Sasaki Masayuki,Kure Shigeo
Funder
the Biomedical Research Core of the Tohoku University Graduate School of Medicine
Biomedical Research Unit of Tohoku University Hospital
Japan Agency for Medical Research and Development
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS;Bonnefond;Biochemistry,2005
2. The role of tRNA synthetases in neurological and neuromuscular disorders;Boczonadi;FEBS Lett,2018
3. Mutation in the nuclear-encoded mitochondrial isoleucyl-tRNA synthetase IARS2 in patients with cataracts, growth hormone deficiency with short stature, partial sensorineural deafness, and peripheral neuropathy or with Leigh syndrome;Schwartzentruber;Hum Mutat,2014
4. Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2;Moosa;Am J Med Genet A,2017
5. Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial disease;Davis;Neurology (in English),2013
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