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...

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Dades bibliogràfiques
Publicat a:	EMBO J
Autors principals:	Tagliavini, F, Prelli, F, Ghiso, J, Bugiani, O, Serban, D, Prusiner, S B, Farlow, M R, Ghetti, B, Frangione, B
Format:	Artigo
Idioma:	Inglês
Publicat:	Nature Publishing Group 1991
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC452678/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1672107/ https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1991.tb07977.x
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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.

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