Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

C. Jansen, P. Parchi, S. Capellari, A.J. Vermeij, P. Corrado, F. Baas, R. Strammiello, W.A. van Gool, J.C. van Swieten, A.J. Rozemuller

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)189-197
Number of pages9
JournalActa Neuropathologica
Volume119
Issue number2
Publication statusPublished - 2010

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