(Q54786905)

English

LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity.

scientific article

LRRK2 G2019S and R1441G mutations associated with Parkinson’s disease are common in the Basque Country, but relative prevalence is determined by ethnicity

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

LRRK2 G2019S and R1441G mutations associated with Parkinson's disease are common in the Basque Country, but relative prevalence is determined by ethnicity (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Parkinson's disease

1 reference

based on heuristic

inferred from title

Adolfo López de Munain

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

José Félix Martí Massó

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

A Gorostidi

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

J Ruiz-Martínez

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

A Alzualde

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

publication date

20 November 2008

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

157-159

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19020907%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0162-0

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the G2019S LRRK2 mutation common in all southern European populations?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19020907

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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