LRRK2G2019S mutations are associated with an increased cancer risk in Parkinson disease-Reference-Cited by-同舟云学术

LRRK2G2019S mutations are associated with an increased cancer risk in Parkinson disease

Published:2010-09-03 Issue:15 Volume:25 Page:2536-2541
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Saunders-Pullman Rachel,Barrett Matthew J.,Stanley Kaili M.,Luciano Marta San,Shanker Vicki,Severt Lawrence,Hunt Ann,Raymond Deborah,Ozelius Laurie J.,Bressman Susan B.

Funder

National Institute of Neurological Disorders and Stroke

Michael J. Fox Foundation

Thomas Hartman Foundation for Parkinson's Research

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference37 articles.

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

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

4. Autosomal dominant parkinsonism associated with variable synuclein and tau pathology;Wszolek;Neurology,2004

5. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews;Ozelius;N Engl J Med,2006

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