Gerstmann–Straussler–Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy. (17th November 2017)

Record Type:: Journal Article
Title:: Gerstmann–Straussler–Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy. (17th November 2017)
Main Title:: Gerstmann–Straussler–Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy
Authors:: Mumoli, L.
Labate, A.
Gambardella, A.
Abstract:
Is Part Of:: European journal of neurology. Volume 24:Number 12(2017:Dec.)
Journal:: European journal of neurology
Issue:: Volume 24:Number 12(2017:Dec.)
Issue Display:: Volume 24, Issue 12 (2017)
Year:: 2017
Volume:: 24
Issue:: 12
Issue Sort Value:: 2017-0024-0012-0000
Page Start:: e87
Page End:: e88
Publication Date:: 2017-11-17
Subjects:: cerebellar atrophy -- inherited prion disease -- PRNP gene -- progressive myoclonic epilepsies
Neurology -- Periodicals
Nervous system -- Diseases -- Periodicals
616.8
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1468-1331 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ene.13447 ↗
Languages:: English
ISSNs:: 1351-5101
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3829.731680
British Library DSC - BLDSS-3PM
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Ingest File:: 5456.xml