Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

Benzer Materyaller

• Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
  Yazar:: Giaccone, G, ve diğerleri
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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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• PET of Brain Prion Protein Amyloid in Gerstmann–Sträussler–Scheinker Disease
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• An autopsy report of three kindred in a Gerstmann–Sträussler–Scheinker disease P105L family with a special reference to prion protein, tau, and beta‐amyloid
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• A Case of Gerstmann-Sträussler-Scheinker Disease
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  Baskı/Yayın Bilgisi: (2010)