LRRK2 exonic variants and risk of multiple system atrophy. - Wikidata - awgldk - TriplyDB

LRRK2 exonic variants and risk of multiple system atrophy.

LRRK2 exonic variants and risk of multiple system atrophy.

http://www.wikidata.org/entity/Q34777870

about

Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders Multiple system atrophy: the application of genetics in understanding etiology.Genetic susceptibility variants in parkinsonism.Multiple system atrophy: pathogenic mechanisms and biomarkers.LRRK2 and the Immune System.MAPT haplotype diversity in multiple system atrophy Selective LRRK2 kinase inhibition reduces phosphorylation of endogenous Rab10 and Rab12 in human peripheral mononuclear blood cells.Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.Multiple System Atrophy: An Oligodendroglioneural Synucleinopathy.Functional Variant rs3135500 in NOD2 Increases the Risk of Multiple System Atrophy in a Chinese Population.

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LRRK2 exonic variants and risk of multiple system atrophy.

http://www.wikidata.org/entity/Q34777870

description

2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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name

LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

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type

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LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

@nl

prefLabel

LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

@en

LRRK2 exonic variants and risk of multiple system atrophy.

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LRRK2 exonic variants and risk of multiple system atrophy.

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Alexandra I Soto-Ortolaza

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Anna Sailer

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David M A Mann

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Dennis W Dickson

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Henry Houlden

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Janice L Holton

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Kiely Aoife

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Kotaro Ogaki

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

Lucia Schottlaender

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

Matthew J Farrer

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

P2860

Second consensus statement on the diagnosis of multiple system atrophy

Score tests for association between traits and haplotypes when linkage phase is ambiguous

Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan.

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy

The neuropathology, pathophysiology and genetics of multiple system atrophy.

Role of mendelian genes in "sporadic" Parkinson's disease.

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.

SNCA variants are associated with increased risk for multiple system atrophy.

Update on novel familial forms of Parkinson's disease and multiple system atrophy.

Reply to: SNCA variants are associated with increased risk of multiple system atrophy.

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2256-2261

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scholarly article

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24

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Melissa E. Murray

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Patrick F. Chinnery

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