(Q81094185)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

LRRK2 is not a significant cause of Parkinson's disease in French-Canadians (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference

7

Guy A Rouleau

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

4

Pierre Provencher

1 reference

5 January 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

Emmanuelle Pourcher

5

object named as

Emmanuelle Pourcher

1 reference

5 January 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

author name string

Nicolas Dupré

1

1 reference

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5 January 2020

Jean-Baptiste Rivière

2

1 reference

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5 January 2020

Richard H Myers

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

François Emond

6

1 reference

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5 January 2020

publication date

1 August 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

Canadian Journal of Neurological Sciences

5 January 2020

published in

1 reference

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5 January 2020

volume

34

1 reference

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5 January 2020

issue

3

1 reference

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5 January 2020

page(s)

333-335

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

5 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

The genetics of Parkinson disease: Implications for neurological care

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

Lrrk2 pathogenic substitutions in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

Neurofilament M gene in a French-Canadian population with Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100006776

7 January 2021

10.1017/S0317167100006776

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17803032%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference