P33. A case of developmental encephalopathy caused by a de novo KCNB1 gene mutation

dc.contributor.author	Terrone, Gaetano
dc.contributor.author	Romano, Adele
dc.contributor.author	Gennaro, Elena
dc.contributor.author	Taglialatela, Maurizio
dc.contributor.author	Del Giudice, Ennio
dc.contributor.author	Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples>
dc.date.accessioned	2020-06-18T06:59:26Z
dc.date.available	2020-06-18T06:59:26Z
dc.date.issued	2019
dc.identifier.citation	Terrone G, Romano A, Gennaro E, Taglialatela M, Del Giudice E. P33. A case of developmental encephalopathy caused by a de novo KCNB1 gene mutation. [poster presentato a: 8th Annual Meeting of the Neapolitan Brain Group, Naples, 13 December 2018]. Translational Medicine @ UniSa. Volume Special Issue 1(2019): 53.	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/10556/4544
dc.identifier.uri	http://dx.doi.org/10.14273/unisa-2738
dc.format.extent	P. 53	it_IT
dc.language.iso	en	it_IT
dc.source	UniSa. Sistema Bibliotecario di Ateneo	it_IT
dc.title	P33. A case of developmental encephalopathy caused by a de novo KCNB1 gene mutation	it_IT
dc.type	Article	it_IT

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