Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
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HYAL-2-WWOX-SMAD4 Signaling in Cell Death and Anticancer ResponseRARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Hyaluronan activates Hyal-2/WWOX/Smad4 signaling and causes bubbling cell death when the signaling complex is overexpressed.Emerging Mechanisms of Aminoacyl-tRNA Synthetase Mutations in Recessive and Dominant Human Disease.Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia - further expansion of the phenotypic spectrum.Expanding spectrum of RARS2 gene disorders: Myoclonic epilepsy, mental retardation, spasticity, and extrapyramidal features.What's new in pontocerebellar hypoplasia? An update on genes and subtypes.WWOX Phosphorylation, Signaling, and Role in Neurodegeneration
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P2860
Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
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2016年學術文章
@zh-hant
name
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@en
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@nl
type
label
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@en
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@nl
prefLabel
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@en
Novel mutations in WWOX, RARS2 ...... with intellectual disability.
@nl
P2093
P2860
P1476
Novel mutations in WWOX, RARS2 ...... s with intellectual disability
@en
P2093
I Richard Thompson
Samah K Aburahma
Wesal Habbab
P2860
P2888
P304
P356
10.1007/S11011-016-9827-9
P577
2016-04-28T00:00:00Z