Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement.
about
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutationRegulation of mRNA Translation in Neurons-A Matter of Life and Death.POLR3A variants in hereditary spastic paraplegia and ataxia.Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.Wiedemann-Rautenstrauch syndrome: A phenotype analysis.
P2860
Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Transcriptome-wide effects of ...... otype of striatal involvement.
@en
Transcriptome-wide effects of ...... otype of striatal involvement.
@nl
type
label
Transcriptome-wide effects of ...... otype of striatal involvement.
@en
Transcriptome-wide effects of ...... otype of striatal involvement.
@nl
prefLabel
Transcriptome-wide effects of ...... otype of striatal involvement.
@en
Transcriptome-wide effects of ...... otype of striatal involvement.
@nl
P2093
P2860
P50
P356
P1476
Transcriptome-wide effects of ...... otype of striatal involvement.
@en
P2093
Anne-Marie J Shearwood
Ara Kaprelyan
Dimitar N Azmanov
Ganqiang Liu
Ivailo Tournev
Luba Kalaydjieva
Margarita Grudkova
Michael Bynevelt
Teodora Chamova
Vassil Svechtarov
P2860
P304
P356
10.1093/HMG/DDW263
P577
2016-08-09T00:00:00Z