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  1. Genome-wide association study in multiple human prion diseases suggests genetic risk...

    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

    http://iris.ucl.ac.uk/iris/publication/378801/2

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