(Q42610405)

English

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

scientific article published on 27 January 2009

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

author name string

C Pirkevi

1

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

S Lesage

2

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

C Condroyer

3

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

H Tomiyama

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

N Hattori

5

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

S Ertan

6

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

A Brice

7

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

A N Başak

8

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

publication date

27 January 2009

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

271-273

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

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/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19172321

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-009-0173-5

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

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