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Gerstmann–Straussler–Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy
Author(s) -
Mumoli L.,
Labate A.,
Gambardella A.
Publication year - 2017
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/ene.13447
Subject(s) - neurology , medicine , pediatrics , family medicine , psychiatry