Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans-Reference-Cited by-同舟云学术

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

Published:2010-03-02 Issue:10 Volume:19 Page:1998-2004
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Lesage Suzanne¹²,Patin Etienne³,Condroyer Christel¹²,Leutenegger Anne-Louise⁴⁵,Lohmann Ebba¹²,Giladi Nir⁶⁷,Bar-Shira Anat⁸,Belarbi Soraya⁹,Hecham Nassima⁹,Pollak Pierre¹⁰,Ouvrard-Hernandez Anne-Marie¹⁰,Bardien Soraya¹¹,Carr Jonathan¹¹,Benhassine Traki¹²,Tomiyama Hiroyuki¹³,Pirkevi Caroline¹⁴,Hamadouche Tarik¹⁵,Cazeneuve Cécile¹⁶,Basak A. Nazli¹⁴,Hattori Nobutaka¹³,Dürr Alexandra¹²¹⁶,Tazir Meriem⁹,Orr-Urtreger Avi⁸⁷,Quintana-Murci Lluis³,Brice Alexis¹²¹⁶,Agid Y.,Bonnet A.-M.,Borg M.,Brice A.,Broussolle E.,Damier Ph.,Destée A.,Dürr A.,Durif F.,Lohmann E.,Martinez M.,Penet C.,Pollak P.,Rascol O.,Tison F.,Tranchant C.,Troiano A.,Vérin M.,Viallet F.,Vidailhet M.,

Affiliation:

1. INSERM, UMR_S975 (Formerly UMR_S679), Paris, France,

2. Pierre et Marie Curie-Paris 6 University, UMR_S975 CRicm, Pitié-Salpêtrière, Paris, France,

3. Institut Pasteur, Human Evolutionary Genetics, CNRS URA3012, Paris, France,

4. INSERM, U946, Fondation Jean Dausset-CEPH, Paris, France,

5. Paris-Diderot University, Institut Universistaire d'Hématologie, paris, France,

6. Movement Disorders Unit Parkinson Center Department of Neurology and

7. The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel,

8. Genetic Institute, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel,

9. Service de Neurologie, CHU Mustapha, Alger, Algeria,

10. Service de Neurologie, CHU de Grenoble, Grenoble, France,

11. Division of Neurology, University of Stellenbosch, Cape Town, South Africa,

12. Laboratoire de biologie moléculaire, Université de Bab Ezzouar, Alger, Algérie,

13. Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan,

14. Neurodegeneration Research Laboratory, Molecular Biology and Genetics Department, Boğaziçi University, Istanbul, Turkey,

15. Laboratoire de biologie moléculaire, Université M'hamed Bougara, Boumerdes, Algeria and

16. Department of Genetics and Cytogenetics, AP-HP, Pitié-Salpêtrière Hospital, Paris, France

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/10/1998/17249458/ddq081.pdf

Reference45 articles.

1. Prevalence of Parkinson's disease in the elderly: the Rotterdam Study;de Rijk;Neurology,1995

2. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004

3. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004

4. Mutations in LRRK2 as a cause of Parkinson's disease;Giasson;Neurosignals,2008

5. The roles of kinases in familial Parkinson's disease;Cookson;J. Neurosci.,2007

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