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Routledge Ltd

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Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

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

By Grasbon-Frodl E.   Lorenz Holger   Mann U.   Nitsch R.   Windl Otto   Kretzschmar H.  

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Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene

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