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Exome Sequencing in Parkinson’s disease

Exome Sequencing is rapidly becoming a fundamental tool for genetics and functional genomics laboratories. This methodology has enabled the discovery of novel pathogenic mutations causing mendelian diseases that had, until now, remained elusive. In this review we discuss not only how we envisage exo...

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Detalhes bibliográficos
Main Authors: Bras, Jose M, Singleton, Andrew B
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3135730/
https://ncbi.nlm.nih.gov/pubmed/21651510
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2011.01722.x
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