Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.

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dc.contributor.authorPirisinu, Laura
dc.contributor.authorDi Bari, Michele A.
dc.contributor.authorD’Agostino, Claudia
dc.contributor.authorMarcon, Stefano
dc.contributor.authorRiccardi, Geraldina
dc.contributor.authorPoleggi, Anna
dc.contributor.authorCohen, Mark L.
dc.contributor.authorAppleby, Brian S.
dc.contributor.authorGambetti, Pierluigi
dc.contributor.authorGhetti, Bernardino
dc.contributor.authorAgrimi, Umberto
dc.contributor.authorNonno, Romolo
dc.contributor.departmentDepartment of Pathology & Laboratory Medicine, IU School of Medicineen_US
dc.date.accessioned2016-03-31T14:25:38Z
dc.date.available2016-03-31T14:25:38Z
dc.date.issued2016
dc.description.abstractGerstmann-Sträussler-Scheinker disease (GSS) is an inherited neurodegenerative disorder associated with mutations in the prion protein gene and accumulation of misfolded PrP with protease-resistant fragments (PrPres) of 6–8 kDa.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationPirisinu, L., Bari, M. A. D., D’Agostino, C., Marcon, S., Riccardi, G., Poleggi, A., … Nonno, R. (2016). Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases. Scientific Reports, 6, 20443. http://doi.org/10.1038/srep20443en_US
dc.identifier.issn2045-2322en_US
dc.identifier.urihttps://hdl.handle.net/1805/9112
dc.language.isoen_USen_US
dc.publisherNPGen_US
dc.relation.isversionof10.1038/srep20443en_US
dc.relation.journalScientific Reportsen_US
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectGerstmann-Sträussler-Scheinker diseaseen_US
dc.subjectneurodegenerative disordersen_US
dc.subject6-8 kDaen_US
dc.titleGerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.en_US
dc.typeArticleen_US
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