Mutation analysis ofParkin,PINK1,DJ-1andATP13A2genes in Chinese patients with autosomal recessive early-onset Parkinsonism-Reference-Cited by-同舟云学术

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Mutation analysis ofParkin,PINK1,DJ-1andATP13A2genes in Chinese patients with autosomal recessive early-onset Parkinsonism

Published:2008-10-30 Issue:14 Volume:23 Page:2074-2079
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Guo Ji-Feng,Xiao Bin,Liao Bing,Zhang Xue-Wei,Nie Li-Luo,Zhang Yu-Hu,Shen Lu,Jiang Hong,Xia Kun,Pan Qian,Yan Xin-Xiang,Tang Bei-Sha

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference24 articles.

1. Mutations in the parkin gene cause autosomal recessive juvenile Parkinsonism;Kitada;Nature,1998

2. Hereditary early-onset Parkinson's disease caused by mutations in PINK1;Valente;Science,2004

3. Mutations in the DJ-1 gene associated with autosomal recessive early-onset Parkinsonism;Bonifati;Science,2003

4. Hereditary Parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase;Ramirez;Nat Genet,2006

5. Association between early-onset Parkinson's disease and mutation in the parkin gene;Lucking;N Engl J Med,2000

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