LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs

被引：443
作者：
Lesage, S [1 ]
Dürr, A
Tazir, M
Lohmann, E
Leutenegger, AL
Janin, S
Pollak, P
Brice, A
机构：
[1] INSERM, U679, F-75651 Paris 13, France
[2] CHU Mustapha, Algiers 16000, Algeria
[3] CHU Grenoble, F-38000 Grenoble, France
来源：
NEW ENGLAND JOURNAL OF MEDICINE | 2006年 / 354卷 / 04期
关键词：
D O I：
10.1056/NEJMc055540
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：422 / 423
页数：2
相关论文
共 8 条
[1]   Genetics of Parkinson's disease: LRRK2 on the rise [J].
Brice, A .
BRAIN, 2005, 128 :2760-2762
[2]   Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism:: Evidence of a common founder across European populations [J].
Kachergus, J ;
Mata, IF ;
Hulihan, M ;
Taylor, JP ;
Lincoln, S ;
Aasly, J ;
Gibson, JM ;
Ross, OA ;
Lynch, T ;
Wiley, J ;
Payami, H ;
Nutt, J ;
Maraganore, DM ;
Czyzewski, K ;
Styczynska, M ;
Wszolek, ZK ;
Farrer, MJ ;
Toft, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (04) :672-680
[3]   G2019S LRRK2 mutation in French and North African families with Parkinson's disease [J].
Lesage, S ;
Ibanez, P ;
Lohmann, E ;
Pollak, P ;
Tison, F ;
Tazir, M ;
Leutenegger, AL ;
Guimaraes, J ;
Bonnet, AM ;
Agid, Y ;
Dürr, A ;
Brice, A .
ANNALS OF NEUROLOGY, 2005, 58 (05) :784-787
[4]   LRRK2 haplotype analyses in European and North African families with Parkinson disease:: A common founder for the G2019S mutation dating from the 13th century [J].
Lesage, S ;
Leutenegger, AL ;
Ibanez, P ;
Janin, S ;
Lohmann, E ;
Dürr, A ;
Brice, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (02) :330-332
[5]   Association between early-onset Parkinson's disease and mutations in the parkin gene [J].
Lücking, CB ;
Dürr, A ;
Bonifati, V ;
Vaughan, J ;
De Michele, G ;
Gasser, T ;
Harhangi, BS ;
Meco, G ;
Denèfle, P ;
Wood, NW ;
Agid, Y ;
Brice, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (21) :1560-1567
[6]   LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews [J].
Ozelius, LJ ;
Senthil, G ;
Saunders-Pullman, R ;
Ohmann, E ;
Deligtisch, A ;
Tagliati, M ;
Hunt, AL ;
Klein, C ;
Henick, B ;
Hailpern, SM ;
Lipton, RB ;
Soto-Valencia, J ;
Risch, N ;
Bressman, SB .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (04) :424-425
[7]   LRRK2 gene in Parkinson disease -: Mutation analysis and case control association study [J].
Paisán-Ruíz, C ;
Lang, AE ;
Kawarai, T ;
Sato, C ;
Salehi-Rad, S ;
Fisman, GK ;
Al-Khairallah, T ;
George-Hyslop, S ;
Singleton, A ;
Rogaeva, E .
NEUROLOGY, 2005, 65 (05) :696-700
[8]   Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity [J].
West, AB ;
Moore, DJ ;
Biskup, S ;
Bugayenko, A ;
Smith, WW ;
Ross, CA ;
Dawson, VL ;
Dawson, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (46) :16842-16847
1