LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century (Q43004241)

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scientific article published in August 2005

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English	LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century	scientific article published in August 2005

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instance of

scholarly article

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stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

title

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

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

main subject

Parkinson's disease

1 reference

based on heuristic

inferred from title

author

Suzanne Lesage

series ordinal

1

object named as

Suzanne Lesage

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

French Parkinson's Disease Genetics Study Group

series ordinal

8

object named as

French Parkinson's Disease Genetics Study Group

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

Sabine Janin Bs

series ordinal

4

object named as

Sabine Janin

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

Ebba Lohmann

series ordinal

5

object named as

Ebba Lohmann

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

Alexandra Durr

series ordinal

6

object named as

Alexandra Dürr

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

Alexis Brice

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7

object named as

Alexis Brice

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

Anne-Louise Leutenegger

series ordinal

2

object named as

Anne-Louise Leutenegger

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

author name string

Pablo Ibanez

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

language of work or name

English

0 references

publication date

1 August 2005

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

volume

77

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

issue

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

page(s)

330-332

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

26 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

16 August 2018

Estimating the age of rare disease mutations: the example of Triple-A syndrome.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1224537

retrieved

16 August 2018

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16145815

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1086/432422

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

PMC publication ID

1224537

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

PubMed publication ID

16145815

1 reference

stated in

Europe PubMed Central

PMC publication ID

1224537

retrieved

12 November 2017

ResearchGate publication ID

7615259

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