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 (...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Oxford University Press 2012
विषय:
Association Studies Articles
ऑनलाइन पहुंच: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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