Rare GCH1 heterozygous variants contributing to Parkinson’s disease-Reference-Cited by-同舟云学术

Rare GCH1 heterozygous variants contributing to Parkinson’s disease

Published:2017-06-03 Issue:7 Volume:140 Page:e41-e41
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Xu Qian¹²,Li Kai¹,Sun Qiying¹²,Ding Dongxue¹,Zhao Yuwen¹,Yang Nannan¹,Luo Yang¹,Liu Zhenhua¹,Zhang Yuan¹,Wang Chunrong¹,Xia Kun²,Yan Xinxiang¹,Jiang Hong¹²³⁴,Shen Lu¹²³⁴,Tang Beisha¹²³⁴⁵,Guo Jifeng¹²³⁴

Affiliation:

1. Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, P.R. China

2. National Clinical Research Center for Geriatric Disorders, Central South University, Changsha, Hunan, P.R. China

3. State Key Laboratory of Medical Genetics, Central South University, Changsha, Hunan, P.R. China

4. Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, P.R. China

5. Parkinson’s Disease Center of Beijing Institute for Brain Disorders, Beijing, P.R. China

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/140/7/e41/18184527/awx110.pdf

Reference16 articles.

1. Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia;Furukawa;Brain,2015

2. Parkinsonism in GTP cyclohydrolase 1 mutation carriers;Guella;Brain,2015

3. A case of parkinsonism and dopa-induced severe dyskinesia associated with novel mutation in the GTP cyclohydrolase I gene;Irie;Parkinsonism Relat Disord,2011

4. Novel GCH1 variant in Dopa-responsive dystonia and Parkinson’s disease;Lewthwaite;Parkinsonism Relat Disord,2015

5. Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers;Mencacci;Brain,2014

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