(Q33377437)

26 July 2017

title

Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3. (English)

1 reference

26 July 2017

1 reference

5

John Hardy

1 reference

26 July 2017

6

Andrew Singleton

1 reference

26 July 2017

4

Rufus Akinyemi

1 reference

26 July 2017

3

Cynthia Crews

1 reference

26 July 2017

1

Njideka Okubadejo

1 reference

26 July 2017

Angela Britton

2

1 reference

26 July 2017

Jose Bras

series ordinal

7

1 reference

26 July 2017

language of work or name

English

0 references

publication date

17 October 2008

1 reference

26 July 2017

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26 July 2017

volume

3

1 reference

26 July 2017

issue

10

1 reference

26 July 2017

page(s)

e3421

1 reference

Creative Commons CC0 License

26 July 2017

copyright license

start time

17 October 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

0 references

cites work

An analysis of genetic studies of Parkinson's disease in Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Deciphering the role of heterozygous mutations in genes associated with parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

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=2559870

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=2559870

S-nitrosylation of parkin regulates ubiquitination and compromises parkin's protective function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

The Unified Parkinson's Disease Rating Scale (UPDRS): status and recommendations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Accounting for human polymorphisms predicted to affect protein function

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Association between early-onset Parkinson's disease and mutations in the parkin gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

Mutation in the alpha-synuclein gene identified in families with 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=2559870

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003421

Parkin variants in North American Parkinson's disease: cases and controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003421

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003421

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003421

Parkinsonism: onset, progression, and mortality. 1967.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2559870

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

31 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003421

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18927607

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genomewide SNP assay reveals mutations underlying Parkinson disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18927607

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18927607

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0003421

1 reference

26 July 2017

0 references

1 reference

26 July 2017

1 reference