A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report
-
* Corresponding author: Ramón A Juste rjuste@neiker.net
BMC Neurology 2010, 10:99 doi:10.1186/1471-2377-10-99
No comments have yet been made on this article.