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Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson’s disease and meta-analysis of the literature

  • Published:2016-08 Issue: Volume:29 Page:42-46
  • ISSN:1353-8020
  • Container-title:Parkinsonism & Related Disorders
  • language:en
  • Short-container-title:Parkinsonism & Related Disorders

Author:

Yang Xinglong,Zhao Quanzhen,An Ran,Zheng JinHua,Tian Sijia,Chen Yalan,Xu Yanming

Funder

Sichuan Key Project of Science and Technology

Sichuan Province Applied Basic Research Program

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference22 articles.

1. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update;Nuytemans;Hum. Mutat.,2010

2. Advances in the genetics of Parkinson disease;Trinh;Nat. Rev. Neurol.,2013

3. Early-onset autosomal-recessive parkinsonian-pyramidal syndrome;Lai;Acta Neurol. Taiwan,2012

4. Genetics of Parkinson’s disease: the yield;Spatola;Park. Relat. Disord.,2014

5. CHCHD2 mutations in autosomal dominant late-onset Parkinson’s disease: a genome-wide linkage and sequencing study;Funayama;Lancet Neurol.,2015

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