A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype-Reference-Cited by-同舟云学术

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A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype

Published:2009-01-27 Issue:3 Volume:10 Page:271-273
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Pirkevi C.,Lesage S.,Condroyer C.,Tomiyama H.,Hattori N.,Ertan S.,Brice A.,Başak A. N.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-009-0173-5.pdf

Reference8 articles.

1. Healy DG, Falchi M, O’Sullivan S et al (2008) Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson’s disease: a case-control study. Lancet Neurol 7:583–590

2. Hulihan MM, Ishihara-Paul L, Kachergus J et al (2008) LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Lancet Neurol 7:591–594

3. Zabetian CP, Hutter CM, Yearout D et al (2006) 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. Am J Hum Genet 79:752–758

4. Kachergus J, Mata IF, Hulihan M et al (2005) Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am J Hum Genet 76(4):672–680

5. Lesage S, Dürr A, Tazir M et al (2006) LRRK2 G2019S as a cause of Parkinson’s disease in North African Arabs. N Engl J Med 354(4):422–423

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Impaired Sonic Hedgehog Responsiveness of Induced Pluripotent Stem Cell-Derived Floor Plate Cells Carrying the LRRK2-I1371V Mutation Contributes to the Ontogenic Origin of Lower Dopaminergic Neuron Yield;Stem Cells and Development;2024-06-01

2. G2019S Variation in LRRK2: An Ideal Model for the Study of Parkinson’s Disease?;Frontiers in Human Neuroscience;2019-09-04

3. Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey;Parkinsonism & Related Disorders;2018-03

4. Evidence for prehistoric origins of the G2019S mutation in the North African Berber population;PLOS ONE;2017-07-19

5. Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson’s Disease;Advances in Neurobiology;2017

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