Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

OBJECTIVE: Recently, vacuolar protein sorting 35 (VPS35) and eukaryotic translation initiation factor 4 gamma 1 (EIF4G1) have been identified as 2 causal Parkinson disease (PD) genes. We used whole exome sequencing for rapid, parallel analysis of variations in these 2 genes. METHODS: We performed wh...

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Detalhes bibliográficos
Main Authors: Nuytemans, Karen, Bademci, Guney, Inchausti, Vanessa, Dressen, Amy, Kinnamon, Daniel D., Mehta, Arpit, Wang, Liyong, Züchner, Stephan, Beecham, Gary W., Martin, Eden R., Scott, William K., Vance, Jeffery M.
Formato: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3653206/
https://ncbi.nlm.nih.gov/pubmed/23408866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e31828727d4
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