Dopa-responsive dystonia in Chinese patients: Including a novel heterozygous mutation in the GCH1 gene with an intermediate phenotype and one case of prenatal diagnosis-Reference-Cited by-同舟云学术

Dopa-responsive dystonia in Chinese patients: Including a novel heterozygous mutation in the GCH1 gene with an intermediate phenotype and one case of prenatal diagnosis

Published:2017-03 Issue: Volume:644 Page:48-54
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Zhang Wen,Zhou Zhizi,Li Xiuzhen,Huang Yonglan,Li Taolin,Lin Yunting,Shao Yongxian,Hu Hao,Liu Hongsheng,Liu Li

Funder

National Natural Science Foundation of China

Major Medical Collaboration and Innovation Program of Guangzhou Science Technology and Innovation Commission

Publisher

Elsevier BV

Subject

General Neuroscience

Reference26 articles.

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3. Monoamine neurotransmitter deficiencies;Pearl;Handb. Clin Neurol.,2013

4. Genetics in dystonia;Klein;Parkinsonism Relat. Disord.,2014

5. Clinical spectrum of dopa-responsive dystonia and related disorders;Lee;Curr. Neurol. Neurosci. Rep.,2014

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