Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations-Reference-Cited by-同舟云学术

Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations

Published:2015-05-07 Issue:7 Volume:30 Page:904-908
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Pont-Sunyer Claustre¹,Bressman Susan²³,Raymond Deborah²,Glickman Amanda²,Tolosa Eduardo¹,Saunders-Pullman Rachel²³

Affiliation:

1. Parkinson Disease and Movement Disorders Unit, Neurology Service, IDIBAPS, CIBERNED; Universitat de Barcelona, Hospital Clínic; Barcelona Catalonia Spain

2. Department of Neurology; Mount Sinai Beth Israel Medical Center; New York NY USA

3. Department of Neurology, Icahn School of Medicine; Mount Sinai Medical Center; New York NY USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.26250/fullpdf

Reference39 articles.

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2. Reply to L. Battistuzzi et al;Lolkema;J Clin Oncol,2013

3. Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants;Alcalay;Genet Med,2014

4. The Clinical Laboratory Improvement Amendments of 1988;4;Health Care Financ Rev,1989

5. Genetic testing legislation in Western Europe: a fluctuating regulatory target;Soini;J Commun Genet,2012

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