TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease? - Test2 - elhamkhani - TriplyDB

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

http://www.wikidata.org/entity/Q39343247

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New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.The Role of TMEM230 Gene in Parkinson's Disease

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P2860

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

http://www.wikidata.org/entity/Q39343247

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@en

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@nl

type

label

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@en

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@nl

prefLabel

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@en

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@nl

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Movement Disorders

P1476

TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease?

@en

P2093

Marialuisa Quadri

http://www.w3.org/2001/XMLSchema#string

Wim Mandemakers

http://www.w3.org/2001/XMLSchema#string

P2860

RME-8 coordinates the activity of the WASH complex with the function of the retromer SNX dimer to control endosomal tubulation.

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

Identification of TMEM230 mutations in familial Parkinson's disease

DNAJC13 mutations in Parkinson disease

Genetics of Parkinson's disease--state of the art, 2013.

VPS35 mutations in Parkinson disease

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease.

Understanding Dopaminergic Cell Death Pathways in Parkinson Disease.

Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population.

P304

1159-1162

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scholarly article

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10.1002/MDS.27061

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P407

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8

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32

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Vincenzo Bonifati

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2017-06-01T00:00:00Z

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28568905

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