Rare coding SNP in DZIP1 gene associated with late-onset sporadic Parkinson's disease

An association between a rare, coding, non-synonymous SNP variant in the gene DZIP1 and Parkinson's disease was found, based on an analysis of the existing NGRC genome-wide association study dataset. The statistical analysis utilized the hypothesis-rich, targeted search unbiased assessment appr...

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Detalles Bibliográficos
Autores principales: Valente, André X. C. N., Shin, Joo H., Sarkar, Abhijit, Gao, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277088/
https://www.ncbi.nlm.nih.gov/pubmed/22355768
http://dx.doi.org/10.1038/srep00256

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277088/
https://www.ncbi.nlm.nih.gov/pubmed/22355768
http://dx.doi.org/10.1038/srep00256

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