GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia-Reference-Cited by-同舟云学术

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GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia

Published:2017-12 Issue: Volume:45 Page:81-84
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Dobričić Valerija,Tomić Aleksandra,Branković Vesna,Kresojević Nikola,Janković Milena,Westenberger Ana,Rašić Vedrana Milić,Klein Christine,Novaković Ivana,Svetel Marina,Kostić Vladimir S.

Funder

Ministry of Education and Science, Republic of Serbia

Hermann and Lilly Schilling Foundation

German Research Foundation (DFG) Research Unit

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference12 articles.

1. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene;Ichinose;Nat. Genet.,1994

2. Dopa-responsive dystonia, Delineation of the clinical syndrome and clues to pathogenesis;Nygaard;Adv. Neurol.,1993

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

4. Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients;Trender-Gerhard;J. Neurol. Neurosurg. Psychiatry,2009

5. Mutations of GCH1 in dopa-responsive dystonia;Müller;Neural. Transm.,2002

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