Condition: Fatal Familial Insomnia


rs74315403 in PRNP gene and Fatal Familial Insomnia PMID 1439789 1992 Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

PMID 1347910 1992 Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178.

PMID 19927125 2010 Conformational diversity in prion protein variants influences intermolecular beta-sheet formation.