Mutant prion protein D202N associated with familial prion disease is retained in the endoplasmic reticulum and forms 'curly' intracellular aggregates.
J Mol Neurosci. 2007;32(1):90-6. doi: 10.1007/s12031-007-0023-6.
J Mol Neurosci. 2007.
PMID: 17873292
Free PMC article.