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.M. Rozemuller

Research output: Contribution to journal/periodicalArticleScientificpeer-review

Original languageEnglish
Pages (from-to)189-197
JournalActa Neuropathologica
Publication statusPublished - 2010

Cite this