Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.

Gerstmann-Sträussler-Scheinker (GSS) disease is a familial neurological disorder pathologically characterized by amyloid deposition in the cerebrum and cerebellum. The GSS amyloid is immunoreactive to antisera raised against the hamster prion protein (PrP) 27-30. This is a proteinase K-resistant gly...

Full description

Saved in:

Bibliographic Details
Main Authors:	Tagliavini, F, Prelli, F, Ghiso, J, Bugiani, O, Serban, D, Prusiner, S B, Farlow, M R, Ghetti, B, Frangione, B
Format:	Artigo
Language:	Inglês
Published:	1991
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC452678/ https://ncbi.nlm.nih.gov/pubmed/1672107
Tags:	Add Tag No Tags, Be the first to tag this record!

Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.

Similar Items