Access
To read this article in full you may need to log in, make a payment or gain access through a site license (see right).
Research Highlights
Nature Reviews Neurology 2, 585 (1 November 2006) | doi:10.1038/ncpneuro0312
Human prion gene polymorphism influences Wilson's disease onset
Abstract
Merle U et al. (2006) Influence of homozygosity for methionine at codon 129 of the human prion gene on the onset of neurological and hepatic symptoms in Wilson disease. Arch Neurol 63: 982–985 Studies indicate that the human prion-related protein (PrP) could be involved in copper homeostasis.
To read this article in full you may need to log in, make a payment or gain access through a site license (see right).
