(Q57983278)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

LRRK2 mutations are a common cause of Parkinson's disease in Spain (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

I F Mata

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

O A Ross

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

J Kachergus

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C Huerta

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

R Ribacoba

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

M Blazquez

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

L M Guisasola

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C Salvador

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

C Martinez

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

V Alvarez

12

1 reference

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20 January 2020

publication date

1 April 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Neurology

20 January 2020

published in

1 reference

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20 January 2020

volume

13

1 reference

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20 January 2020

issue

4

1 reference

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20 January 2020

page(s)

391-394

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

Diagnostic criteria for Parkinson disease

20 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.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.1468-1331.2006.01256.X

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.X

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.X

21 January 2018

The Rab GTPase family

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.X

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.X

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01256.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.1468-1331.2006.01256.X

10.1111/J.1468-1331.2006.01256.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16643318%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference