Article
Prion disease.
Handbook of clinical neurology - 1 Jan 2018
Takada Leonel T, Kim Mee-Ohk, Metcalf Stacy, Gala Ignacio Illán, Geschwind Michael D
Abstract excerpt
Genetic prion diseases (gPrDs) are caused by autosomal-dominant mutations in the prion protein gene (PRNP). Although the first PRNP mutations identified, and most since, are PRNP missense, octapeptide repeat insertions, deletion and nonsense mutations have now also been shown to cause gPrD. Based on clinicopathologic features of familial disease, gPrDs historically have been classified into three forms: familial...
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