A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
about
A novel missense mutation of CMT2P alters transcription machinery.A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.LRSAM1-mediated ubiquitylation is disrupted in axonal Charcot-Marie-Tooth disease 2P.Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1.
P2860
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@ast
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@en
type
label
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@ast
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@en
prefLabel
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@ast
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@en
P2093
P2860
P50
P356
P1476
A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.
@en
P2093
Bart P van de Warrenburg
H Jurgen Schelhaas
Marialuisa Quadri
Marian A J Weterman
Marjolein B Aerts
Rianne A Esselink
P2860
P304
P356
10.1002/ACN3.281
P577
2015-12-22T00:00:00Z