Loss of glycosylation associated with the T183A mutation in human prion disease (Q40488897)

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Loss of glycosylation associated with the T183A mutation in human prion disease
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    Loss of glycosylation associated with the T183A mutation in human prion disease (English)
    E Grasbon-Frodl
    Holger Lorenz
    R M Nitsch
    Otto Windl
    H A Kretzschmar
    26 October 2004
    476-484

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