The genetics of prion diseases

Prion diseases are a rare group of fatal neurodegenerative disorders of humans and animals that manifest primarily as progressive dementia and ataxia. Unique to these diseases is the prion, a misfolded isoform of the prion protein that can transmit disease from cell to cell or host to host by associ...

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Veröffentlicht in:	Genetics in medicine 2010-04, Vol.12 (4), p.187-195
1. Verfasser:	Mastrianni, James A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biomedical and Life Sciences Biomedicine Brain - metabolism Brain - pathology familial CJD FFI genetest-review Genetic Association Studies Genetic Predisposition to Disease genetic prion disease GSS Human Genetics Humans Laboratory Medicine Mutation Polymorphism, Genetic prion Prion Diseases - classification Prion Diseases - genetics Prion Diseases - pathology Prion Proteins Prions - genetics PRNP
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