P13. Inhibition of S1P degradation is beneficial in the transgenic R6/2 mouse model of huntington disease

dc.contributor.author	Di Pardo, Alba
dc.contributor.author	Amico, Enrico
dc.contributor.author	Castaldo, Salvatore
dc.contributor.author	Capocci, Luca
dc.contributor.author	Pepe, Giuseppe
dc.contributor.author	Maglione, Vittorio
dc.contributor.author	Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples>
dc.date.accessioned	2020-06-24T09:22:14Z
dc.date.available	2020-06-24T09:22:14Z
dc.date.issued	2019
dc.identifier.citation	Di 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
dc.identifier.issn	2239-9747	it_IT
dc.identifier.uri	http://www.translationalmedicine.unisa.it/index	it_IT
dc.identifier.uri	http://elea.unisa.it:8080/xmlui/handle/10556/4564
dc.identifier.uri	http://dx.doi.org/10.14273/unisa-2758
dc.format.extent	P. 33	it_IT
dc.language.iso	en	it_IT
dc.source	UniSa. Sistema Bibliotecario di Ateneo	it_IT
dc.title	P13. Inhibition of S1P degradation is beneficial in the transgenic R6/2 mouse model of huntington disease	it_IT
dc.type	Article	it_IT

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