Genomewide SNP assay reveals mutations underlying Parkinson disease-Reference-Cited by-同舟云学术

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Genomewide SNP assay reveals mutations underlying Parkinson disease

Published:2008-02 Issue:2 Volume:29 Page:315-322
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Simon-Sanchez Javier,Scholz Sonja,del Mar Matarin Maria,Fung Hon-Chung,Hernandez Dena,Gibbs J Raphael,Britton Angela,Hardy John,Singleton Andrew

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.20626/fullpdf

Reference19 articles.

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

2. Structural variation in the human genome;Feuk;Nat Rev Genet,2006

3. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data;Fung;Lancet Neurol,2006

4. Application of genome-wide single nucleotide polymorphism typing: simple association and beyond;Gibbs;PLoS Genet,2006

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