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dcterms.contributor.authorDi Pardo, Alba
dcterms.contributor.authorAmico, Enrico
dcterms.contributor.authorCastaldo, Salvatore
dcterms.contributor.authorCapocci, Luca
dcterms.contributor.authorPepe, Giuseppe
dcterms.contributor.authorMaglione, Vittorio
dcterms.contributor.authorAnnual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples>
dc.date.accessioned2020-06-24T09:22:14Z
dc.date.available2020-06-24T09:22:14Z
dcterms.date.issued2019
dcterms.identifier.citationDi Pardo A, Amico E, Castaldo S, Capocci L, Pepe G, Maglione V. P13. Inhibition of S1P degradation is beneficial in the transgenic R6/2 mouse model of huntington disease. [poster presentato a: 8th Annual Meeting of the Neapolitan Brain Group, Naples, 13 December 2018]. Translational Medicine @ UniSa. Volume Special Issue 1(2019): 33.it_IT
dcterms.identifier.issn2239-9747it_IT
dcterms.identifier.urihttp://www.translationalmedicine.unisa.it/indexit_IT
dcterms.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/4564
dcterms.identifier.urihttp://dx.doi.org/10.14273/unisa-2758
dcterms.format.extentP. 33it_IT
dc.language.isoenit_IT
dcterms.sourceUniSa. Sistema Bibliotecario di Ateneoit_IT
dcterms.titleP13. Inhibition of S1P degradation is beneficial in the transgenic R6/2 mouse model of huntington diseaseit_IT
dcterms.typeArticleit_IT
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