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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Bras, Jose M, Singleton, Andrew B
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2011
Schlagworte:
Online Zugang: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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