about
A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease.Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
CHCHD2 and Parkinson's disease.
@en
CHCHD2 and Parkinson's disease.
@nl
type
label
CHCHD2 and Parkinson's disease.
@en
CHCHD2 and Parkinson's disease.
@nl
prefLabel
CHCHD2 and Parkinson's disease.
@en
CHCHD2 and Parkinson's disease.
@nl
P2093
P50
P1433
P1476
CHCHD2 and Parkinson's disease.
@en
P2093
Alexis Brice
Huw Morris
Iris E Jansen
J Raphael Gibbs
Manu Sharma
Mike A Nalls
P304
P356
10.1016/S1474-4422(15)00094-0
P50
P577
2015-07-01T00:00:00Z