PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
about
Emerging Mechanisms of Aminoacyl-tRNA Synthetase Mutations in Recessive and Dominant Human Disease.Human aminoacyl-tRNA synthetases in diseases of the nervous system.Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers.The role of tRNA synthetases in neurological and neuromuscular disorders.A familial case of PDE10A-associated childhood-onset chorea with bilateral striatal lesions.Towards an Integrative Understanding of tRNA Aminoacylation-Diet-Host-Gut Microbiome Interactions in Neurodegeneration.
P2860
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@en
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@nl
type
label
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@en
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@nl
prefLabel
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@en
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@nl
P2093
P2860
P356
P1476
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder.
@en
P2093
Ayelet Eran
Hanna Mandel
Hirotaka Motoi
Kazuhiro Ogata
Keitaro Yamada
Masaaki Shiina
Mitsuko Nakashima
Miyuki Toyono
Naomichi Matsumoto
Nina Ekhilevitch
P2860
P2888
P304
P356
10.1038/JHG.2016.163
P577
2017-01-12T00:00:00Z