A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients-Reference-Cited by-同舟云学术

A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients

Published:2009-04-07 Issue:7 Volume:24 Page:1023-1027
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Shojaee Seyedmehdi,Sina Farzad,Farboodi Niloofar,Fazlali Zeinab,Ghazavi Farzaneh,Ghorashi Seyed Ali,Parsa Khosro,Sadeghi Homa,Shahidi Gholam-Ali,Ronaghi Mostafa,Elahi Elahe

Funder

Iran National Science Foundation

Center of Excellence in Biomathematics

School of Mathematics, University of Tehran

Iranian Studies for Parkinson's Disease

Iran PD genetics

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.22503/fullpdf

Reference20 articles.

1. Prevalence of Parkinson's disease in the elderly: the Rotterdam study;Rijk;Neurology,1995

2. Understanding the molecular causes of Parkinson's disease;Wood-Kaczmar;Trends Mol Med,2006

3. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruız;Neuron,2004

4. Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004

5. Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease;Haugarvoll;Neurology,2008

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