Article ID Journal Published Year Pages File Type
3078817 Neurologic Clinics 2007 10 Pages PDF
Abstract

Prion diseases are a unique group of neurologic diseases caused by an abnormal protein conformation. Prion diseases encompass genetic, sporadic, iatrogenic, and acquired conditions in humans and other mammals. Although they are relatively rare, they produce a diverse array of symptoms, uniformly are fatal, and provide important information about proteins and degenerative neurobiology in addition to lessons about animal and human food chains.

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