Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa-Reference-Cited by-同舟云学术

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa

Published:2010-08-18 Issue:13 Volume:25 Page:2052-2058
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Jasinska-Myga Barbara,Kachergus Jennifer,Vilariño-Güell Carles,Wider Christian,Soto-Ortolaza Alexandra I.,Kefi Mounir,Middleton Lefkos T.,Ishihara-Paul Lianna,Gibson Rachel A.,Amouri Rim,Yahmed Samia Ben,Sassi Samia Ben,Zouari Mourad,Euch Ghada El,Ross Owen A.,Hentati Faycal,Farrer Matthew J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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4. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study;Hulihan;Lancet Neurol,2008

5. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs;Lesage;N Engl J Med,2006

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