LRRK2 haplotype analyses in European and North African families with Parkinson disease:: A common founder for the G2019S mutation dating from the 13th century

被引：108

作者：

Lesage, S

Leutenegger, AL

Ibanez, P

Janin, S

Lohmann, E

Dürr, A

Brice, A

机构：

[1] Hop La Pitie Salpetriere, INSERM, U679, F-75651 Paris, France

[2] Hop La Pitie Salpetriere, Dept Genet, F-75651 Paris, France

[3] CHU Pitie Salpetriere, Federat Neurol, Paris, France

[4] Unite Format & Rech Pierre & Marie Curie, Paris, France

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2005年 / 77卷 / 02期

关键词：

D O I：

10.1086/432422

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：330 / 332

页数：3

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