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

L Mumoli1, A Labate1,2, A Gambardella1,2

  • 1Institute of Neurology, University Magna Graecia, Catanzaro, Italy.

European Journal of Neurology
|November 18, 2017
PubMed
Abstract

No abstract available in PubMed .

Keywords:
PRNP genecerebellar atrophyinherited prion diseaseprogressive myoclonic epilepsies

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