LRRK2 and Parkinson?s disease in Norway (Q57983263)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17419834%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

LRRK2 and Parkinson's disease in Norway (English)

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28 December 2019

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1

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28 December 2019

Kristoffer Haugarvoll

2

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28 December 2019

Matthew J. Farrer

4

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28 December 2019

author name string

O A Ross

3

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28 December 2019

J O Aasly

5

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28 December 2019

language of work or name

English

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publication date

1 January 2007

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Acta neurologica Scandinavica. Supplementum

28 December 2019

published in

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28 December 2019

volume

187

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28 December 2019

issue

s187

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page(s)

72-75

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

28 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

The LRRK2 gene in Parkinson's disease: mutation screening in patients from Germany

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Clinical features of LRRK2-associated Parkinson's disease in central Norway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

LRRK2 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Lrrk2 and Lewy body disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2007.00852.X

10.1111/J.1600-0404.2007.00852.X

21 January 2018

Identifiers

DOI

1 reference

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28 December 2019

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