(Q33267533)

24 July 2017

title

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan (English)

1 reference

24 July 2017

1 reference

3

John Hardy

1 reference

24 July 2017

4

Andrew B Singleton

1 reference

24 July 2017

Hon-Chung Fung

1

1 reference

24 July 2017

Chiung-Mei Chen

series ordinal

2

1 reference

24 July 2017

Yih-Ru Wu

series ordinal

5

1 reference

24 July 2017

publication date

22 December 2006

1 reference

24 July 2017

1 reference

24 July 2017

volume

6

1 reference

24 July 2017

page(s)

47

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-6-47

24 July 2017

exact match

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

Kinase activity is required for the toxic effects of mutant LRRK2/dardarin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

Prevalence of Parkinson's disease and related disorders in the elderly population of greater Beijing, China

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764029

LRRK2 mutations in Parkinson disease

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2377-6-47

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2377-6-47

Prevalence of Parkinson's disease in China

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17187665

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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/17187665

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17187665

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2377-6-47

1 reference

Dimensions Publication ID

24 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-6-47

9 September 2019

1 reference

24 July 2017

1 reference