(Q33603103)

28 July 2017

title

LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patients (English)

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28 July 2017

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6

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Suzanne Lesage

series ordinal

5

object named as

Suzanne Lesage

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28 July 2017

1

Soraya Bardien

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28 July 2017

7

Jonathan Carr

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28 July 2017

Angelica Marsberg

2

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28 July 2017

Rowena Keyser

series ordinal

3

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28 July 2017

Debbie Lombard

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4

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28 July 2017

publication date

11 June 2010

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Journal of Neural Transmission

28 July 2017

published in

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28 July 2017

volume

117

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28 July 2017

issue

7

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28 July 2017

page(s)

847-853

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https://scigraph.springernature.com/pub.10.1007/s00702-010-0423-6

28 July 2017

exact match

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cites work

A comparison of clinical and pathological features of young- and old-onset Parkinson's disease

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Crossref

https://api.crossref.org/works/10.1007%2FS00702-010-0423-6

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

21 January 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS00702-010-0423-6

The Roco protein family: a functional perspective

21 January 2018

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12 December 2020

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans

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12 December 2020

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

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12 December 2020

High resolution melting applications for clinical laboratory medicine

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12 December 2020

LRRK2 R1628P increases risk of Parkinson's disease: replication evidence

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12 December 2020

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

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12 December 2020

Risk tables for parkinsonism and Parkinson's disease.

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12 December 2020

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

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12 December 2020

Leucine-rich repeat kinase 2: relevance to Parkinson's disease

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12 December 2020

Co-occurrence of sporadic parkinsonism and late-onset Alzheimer's disease in a Brazilian male with the LRRK2 p.G2019S mutation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations

1 reference

12 December 2020

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

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12 December 2020

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

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12 December 2020

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

1 reference

12 December 2020

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

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12 December 2020

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

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12 December 2020

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.

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12 December 2020

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

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12 December 2020

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

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12 December 2020

Genetic structure of a unique admixed population: implications for medical research

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12 December 2020

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

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12 December 2020

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

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12 December 2020

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

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12 December 2020

Parkinson's disease: from monogenic forms to genetic susceptibility factors

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12 December 2020

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

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12 December 2020

High-resolution genotyping by amplicon melting analysis using LCGreen

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12 December 2020

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

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12 December 2020

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

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12 December 2020

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

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12 December 2020

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

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12 December 2020

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.

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12 December 2020

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

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12 December 2020

Mutations in LRRK2 as a cause of Parkinson's disease

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12 December 2020

Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group

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12 December 2020

Roc, a Ras/GTPase domain in complex proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00702-010-0423-6

Identifiers

DOI

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28 July 2017

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