GCH1 in early-onset Parkinson's disease-Reference-Cited by-同舟云学术

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GCH1 in early-onset Parkinson's disease

Published:2009-09-04 Issue:14 Volume:24 Page:2070-2075
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Cobb Stephanie A.,Wider Christian,Ross Owen A.,Mata Ignacio F.,Adler Charles H.,Rajput Alex,Rajput Ali H.,Wu Ruey-Meei,Hauser Robert,Josephs Keith A.,Carr Jonathan,Gwinn Katrina,Heckman Michael G.,Aasly Jan O.,Lynch Timothy,Uitti Ryan J.,Wszolek Zbigniew K.,Kapatos Gregory,Farrer Matthew J.

Funder

Swiss National Science Foundation

Swiss Parkinson Foundation

Simpson Foundation Trust

Center of Excellence for Parkinson's disease Research

Pacific Alzheimer Research Foundation

NINDS

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.22729/fullpdf

Reference25 articles.

1. Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease);Segawa;Ann Neurol,2003

2. Update on dopa-responsive dystonia: locus heterogeneity and biochemical features;Furukawa;Adv Neurol,2004

3. Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1: redefining DYT14 as DYT5;Wider;Neurology,2008

4. Dopa-responsive dystonia: the spectrum of clinical manifestations in a large North American family;Nygaard;Neurology,1990

5. Gender-related penetrance and de novo GTP-cyclohydrolase I gene mutations in dopa-responsive dystonia;Furukawa;Neurology,1998

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