Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy

Academic Article

Publication Date:

2017

Iris type:

01.08 Comunicazione in rivista (Letter - Letter to editor)

Keywords:

cerebellar atrophy; inherited prion disease; PRNP gene; progressive myoclonic epilepsies

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