LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews

被引：536

作者：

Ozelius, LJ ^{[1
]}

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

机构：

[1] Albert Einstein Coll Med, Bronx, NY 10461 USA

[2] Beth Israel Med Ctr, New York, NY 10003 USA

[3] Med Univ Lubeck, D-23538 Lubeck, Germany

[4] Univ Calif San Francisco, San Francisco, CA 94143 USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2006年 / 354卷 / 04期

关键词：

D O I：

10.1056/NEJMc055509

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：424 / 425

页数：2

共 8 条

[1] How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease
Cookson, MR
Xiromerisiou, G
Singleton, A
[J]. CURRENT OPINION IN NEUROLOGY, 2005, 18 (06) : 706 - 711
[2] Genetics of Parkinson's disease
Gasser, T
[J]. CURRENT OPINION IN NEUROLOGY, 2005, 18 (04) : 363 - 369
[3] The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases
Hernandez, D
Ruiz, CP
Crawley, A
Malkani, R
Werner, J
Gwinn-Hardy, K
Dickson, D
DeVrieze, FW
Hardy, J
Singleton, A
[J]. NEUROSCIENCE LETTERS, 2005, 389 (03) : 137 - 139
[4] 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
[5] LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
Lesage, S
Dürr, A
Tazir, M
Lohmann, E
Leutenegger, AL
Janin, S
Pollak, P
Brice, A
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (04) : 422 - 423
[6] 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
[7] Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations
Pankratz, N
Nichols, WC
Uniacke, SK
Halter, C
Rudolph, A
Shults, C
Conneally, PM
Foroud, T
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (01) : 124 - 135
[8] GENETIC-ANALYSIS OF IDIOPATHIC TORSION DYSTONIA IN ASHKENAZI JEWS AND THEIR RECENT DESCENT FROM A SMALL FOUNDER POPULATION
RISCH, N
DELEON, D
OZELIUS, L
KRAMER, P
ALMASY, L
SINGER, B
FAHN, S
BREAKEFIELD, X
BRESSMAN, S
[J]. NATURE GENETICS, 1995, 9 (02) : 152 - 159

← 1 →