We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleChildhood onset in familial prion disease with a novel mutation in the PRNP gene.AuthorsRogaeva, Ekaterina; Zadikoff, Cindy; Ponesse, Jonathan; Schmitt-Ulms, Gerold; Kawarai, Toshitaka; Sato, Christine; Salehi-Rad, Shabnam; St George-Hyslop, Peter; Lang, Anthony EAbstractUp to 15% of cases of prion diseases are due to the autosomal dominant inheritance of coding PRNP mutations.PublicationArchives of neurology, 2006, Vol 63, Issue 7, p1016ISSN0003-9942Publication typeJournal ArticleDOI10.1001/archneur.63.7.1016