Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP
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F. Baas | J. V. van Swieten | W. V. van Gool | A. Rozemuller | P. Corrado | S. Capellari | Piero Parchi | R. Strammiello | C. Jansen | A. Vermeij