Familial genes in sporadic disease: Common variants of α-synuclein gene associate with Parkinson's disease-Reference-Cited by-同舟云学术

Familial genes in sporadic disease: Common variants of α-synuclein gene associate with Parkinson's disease

Published:2007-05 Issue:5-6 Volume:128 Page:378-382
ISSN:0047-6374
Container-title:Mechanisms of Ageing and Development
language:en
Short-container-title:Mechanisms of Ageing and Development

Author:

Ross Owen A.,Gosal David,Stone Jeremy T.,Lincoln Sarah J.,Heckman Michael G.,Irvine G. Brent,Johnston Janet A.,Gibson J. Mark,Farrer Matthew J.,Lynch Timothy

Publisher

Elsevier BV

Subject

Developmental Biology,Aging

Reference19 articles.

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

3. Effect of allelic variation at the NACP-Rep1 repeat upstream of the alpha-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system;Chiba-Falek;Hum. Mol. Genet.,2001

4. Identification of patterns in biological sequences at the ALGGEN server: PROMO and MALGEN;Farré;Nucleic Acids Res.,2003

5. Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications;Farrer;Ann. Neurol.,2004

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