Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene.
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Acta Neuropathol Commun. 2019 Jan 3;7(1):1. doi: 10.1186/s40478-018-0656-4.
Acta Neuropathol Commun. 2019.
PMID: 30606247
Free PMC article.