Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. (Q54779430)

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• Genetic association study of the P-type ATPaseATP13A2in late-onset Parkinson's disease

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English	Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.	scientific article	Genetic association study of the P-type ATPaseATP13A2in late-onset Parkinson's disease

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scholarly article

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

title

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. (English)

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

main subject

Parkinson's disease

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inferred from title

author

Alfredo Ramirez

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15

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

Peter Nürnberg

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11

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Peter Nürnberg

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

Christine Klein

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13

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Christine Klein

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PubMed publication ID

19097176

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3 June 2018

Katja Lohmann

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9

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Katja Lohmann

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

Vladimir S. Kostić

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8

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Vladimir Kostic

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19097176

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Michael Linnebank

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7

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Michael Linnebank

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author name string

Aleksandar Rakovic

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1

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19097176

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3 June 2018

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Barbara Stiller

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2

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19097176

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3 June 2018

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Ana Djarmati

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3

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19097176

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Antonia Flaquer

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4

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19097176

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Jan Freudenberg

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5

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19097176

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Mohammad-Reza Toliat

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6

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19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

Sebastian Paus

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10

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19097176

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Christian Kubisch

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12

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19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

Ullrich Wüllner

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14

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Europe PubMed Central

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19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

language of work or name

English

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publication date

1 February 2009

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19097176

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3 June 2018

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http://europepmc.org/abstract/MED/19097176

published in

Movement Disorders

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19097176

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3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

volume

24

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

issue

3

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Europe PubMed Central

PubMed publication ID

19097176

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3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

page(s)

429-433

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PubMed publication ID

19097176

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3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

cites work

Parkinson's disease. Second of two parts

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMDS.22399

retrieved

21 January 2018

Parkinson's disease. First of two parts

1 reference

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMDS.22399

retrieved

21 January 2018

Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism

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https://api.crossref.org/works/10.1002%2FMDS.22399

retrieved

21 January 2018

Molecular Pathways of Neurodegeneration in Parkinson's Disease

1 reference

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

Cell biology of protein misfolding: the examples of Alzheimer's and Parkinson's diseases

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Crossref

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

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Crossref

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia

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21 January 2018

ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

HapBlock: haplotype block partitioning and tag SNP selection software using a set of dynamic programming algorithms.

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21 January 2018

A note on exact tests of Hardy-Weinberg equilibrium

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21 January 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

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21 January 2018

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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Crossref

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

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https://api.crossref.org/works/10.1002%2FMDS.22399

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21 January 2018

High-resolution whole-genome association study of Parkinson disease.

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retrieved

21 January 2018

Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease

1 reference

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Crossref

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21 January 2018

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

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Crossref

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https://api.crossref.org/works/10.1002%2FMDS.22399

retrieved

21 January 2018

Identifiers

DOI

10.1002/MDS.22399

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19097176

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

PubMed publication ID

19097176

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19097176

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/19097176

ResearchGate publication ID

23678101

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