(Q35199232)

7 August 2017

title

Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America (English)

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7 August 2017

28

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29

Owen A Ross

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7 August 2017

Carles Vilariño-Güell

15

object named as

Carles Vilariño-Güell

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7 August 2017

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Oscar Acosta

9

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ORCID Public Data File 2021

author name string

Ignacio F Mata

1

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7 August 2017

Greggory J Wilhoite

2

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7 August 2017

Dora Yearout

3

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7 August 2017

Justin A Bacon

4

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Mario Cornejo-Olivas

5

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Pilar Mazzetti

6

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Victoria Marca

7

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Olimpio Ortega

8

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Carlos Cosentino

10

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Luis Torres

11

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Angel C Medina

12

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Carolina Perez-Pastene

13

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Fernando Díaz-Grez

14

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Pablo Venegas

16

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Marcelo Miranda

17

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Osvaldo Trujillo-Godoy

18

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Luis Layson

19

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Rodrigo Avello

20

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Elena Dieguez

21

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Victor Raggio

22

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Federico Micheli

23

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Claudia Perandones

24

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Victoria Alvarez

25

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Juan Segura-Aguilar

26

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Matthew J Farrer

27

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7 August 2017

publication date

31 May 2011

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7 August 2017

number of pages

3

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Parkinsonism and Related Disorders

inferred from page(s)

published in

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7 August 2017

volume

17

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7 August 2017

issue

8

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7 August 2017

page(s)

629-631

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LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

Lrrk2 mutations in South America: A study of Chilean Parkinson's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

Lrrk2 pathogenic substitutions in Parkinson's disease

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3167927

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

15 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21632271

12 December 2020

inferred from PubMed ID database lookup

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21632271

12 December 2020

inferred from PubMed ID database lookup

Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21632271

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.PARKRELDIS.2011.05.003

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7 August 2017

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7 August 2017

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