(Q46741022)

24 December 2017

editorial

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title

Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant (English)

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24 December 2017

2

A H Schapira

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24 December 2017

author name string

E K Tan

series ordinal

1

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24 December 2017

publication date

1 March 2008

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24 December 2017

European Journal of Neurology

published in

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24 December 2017

volume

15

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24 December 2017

issue

3

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24 December 2017

page(s)

203-204

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24 December 2017

Pathogenic mutations in Parkinson disease

cites work

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https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

The importance of LRRK2 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.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.1468-1331.2007.02053.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.1468-1331.2007.02053.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.1468-1331.2007.02053.X

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.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.1468-1331.2007.02053.X

Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.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.1468-1331.2007.02053.X

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.02053.X

10.1111/J.1468-1331.2007.02053.X

21 January 2018

Identifiers

DOI

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24 December 2017

PubMed ID

18290841

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24 December 2017