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Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease

  • Published:2016-03 Issue: Volume:24 Page:89-94
  • ISSN:1353-8020
  • Container-title:Parkinsonism & Related Disorders
  • language:en
  • Short-container-title:Parkinsonism & Related Disorders

Author:

Wang Gang,Huang YueORCID,Wei Chen ,Chen Shuai,Wang Ying,Xiao Qin,Liu Jun,Fung Victor S.C.,Halliday Glenda,Chen Shengdi

Funder

University of New South Wales

NHMRC Senior Principal Research Fellow

National Program of Basic Research of China

National Natural Science Foundation

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference33 articles.

1. Genome-wide association study reveals genetic risk underlying Parkinson's disease;Simon-Sanchez;Nat. Genet.,2009

2. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease;Satake;Nat. Genet.,2009

3. Replication of GWAS associations for GAK and MAPT in Parkinson's disease;Rhodes;Ann. Hum. Genet.,2011

4. Analysis of genome-wide association study-linked loci in Parkinson's disease of Mainland China;Liu;Mov. Disord. official J. Mov. Disord. Soc.,2013

5. Alpha-synuclein locus duplication as a cause of familial Parkinson's disease;Chartier-Harlin;Lancet,2004
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