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

被引：436

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

页码：422 / 423

页数：2

共 8 条

[1] Genetics of Parkinson's disease: LRRK2 on the rise
Brice, A
[J]. 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
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
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (04) : 672 - 680
[3] G2019S LRRK2 mutation in French and North African families with Parkinson's disease
Lesage, S
Ibanez, P
Lohmann, E
Pollak, P
Tison, F
Tazir, M
Leutenegger, AL
Guimaraes, J
Bonnet, AM
Agid, Y
Dürr, A
Brice, A
[J]. 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
Lesage, S
Leutenegger, AL
Ibanez, P
Janin, S
Lohmann, E
Dürr, A
Brice, A
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (02) : 330 - 332
[5] Association between early-onset Parkinson's disease and mutations in the parkin gene
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
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (21) : 1560 - 1567
[6] LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
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
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (04) : 424 - 425
[7] LRRK2 gene in Parkinson disease -: Mutation analysis and case control association study
Paisán-Ruíz, C
Lang, AE
Kawarai, T
Sato, C
Salehi-Rad, S
Fisman, GK
Al-Khairallah, T
George-Hyslop, S
Singleton, A
Rogaeva, E
[J]. NEUROLOGY, 2005, 65 (05) : 696 - 700
[8] Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
West, AB
Moore, DJ
Biskup, S
Bugayenko, A
Smith, WW
Ross, CA
Dawson, VL
Dawson, TM
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (46) : 16842 - 16847

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