The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy. (Q50264526)

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30 January 2020

title

The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy (English)

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3

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Silvio Peluso

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Ben A Oostra

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author name string

Chiara Criscuolo

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Anna De Rosa

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Erik J Simons

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Guido J Breedveld

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Giampiero Volpe

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Alessandro Filla

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Giuseppe De Michele

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Vincenzo Bonifati

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language of work or name

English

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publication date

29 April 2011

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volume

26

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issue

9

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page(s)

1733-1736

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Molecular pathogenesis of Parkinson disease: insights from genetic studies

30 January 2020

cites work

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LRRK2 gene variation and its contribution to Parkinson disease

21 January 2018

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

21 January 2018

1 reference

Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy

21 January 2018

1 reference

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

21 January 2018

1 reference

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

21 January 2018

1 reference

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

21 January 2018

1 reference

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

21 January 2018

1 reference

Environmental and genetic risk factors in Parkinson's disease: a case-control study in southern Italy.

21 January 2018

1 reference

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

21 January 2018

1 reference

A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.

21 January 2018

1 reference

Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.23735

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30 January 2020

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