Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Prion diseases are fatal neurodegenerative diseases of humans and animals caused by the misfolding and aggregation of prion protein (PrP). Mammalian prion diseases are under strong genetic control but few risk factors are known aside from the PrP gene locus (PRNP). No genome-wide association study (...

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Detalhes bibliográficos
Main Authors: Mead, Simon, Uphill, James, Beck, John, Poulter, Mark, Campbell, Tracy, Lowe, Jessica, Adamson, Gary, Hummerich, Holger, Klopp, Norman, Rückert, Ina-Maria, Wichmann, H-Erich, Azazi, Dhoyazan, Plagnol, Vincent, Pako, Wandagi H., Whitfield, Jerome, Alpers, Michael P., Whittaker, John, Balding, David J., Zerr, Inga, Kretzschmar, Hans, Collinge, John
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Association Studies Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3313791/
https://ncbi.nlm.nih.gov/pubmed/22210626
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr607
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