Condition: SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES


rs74315411 in PRNP gene and SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES PMID 12214108 2000 The Thr183Ala Mutation, Not the Loss of the First Glycosylation Site, Alters the Physical Properties of the Prion Protein.

PMID 9266722 1997 Familial spongiform encephalopathy associated with a novel prion protein gene mutation.