Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.
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Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.Proteins and chemical chaperones involved in neuronal nicotinic receptor expression and function: an update.New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Regulation of RIC-3 and of nAChR expression.
P2860
Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.
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
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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
@zh-hant
name
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@en
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@nl
type
label
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@en
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@nl
prefLabel
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@en
Evidence of mutations in RIC3 ...... ase with non-motor phenotypes.
@nl
P2093
P2860
P1476
Evidence of mutations in RIC3 ...... ease with non-motor phenotypes
@en
P2093
Madhuri Behari
Ramesh C Juyal
Shyla T Govindappa
Sumedha Sudhaman
Uday B Muthane
P2860
P304
P356
10.1136/JMEDGENET-2015-103616
P407
P50
P577
2016-04-07T00:00:00Z