Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.
Jansen C; Parchi P; Capellari S; Vermeij AJ; Corrado P; Baas F; Strammiello R; van Gool WA; van Swieten JC; Rozemuller AJ; Acta Neuropathologica, 2010, vol. 119, issue 2, p 189, ISSN 14320533. ISBN 14320533.

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