Please use this identifier to cite or link to this item: http://elea.unisa.it/xmlui/handle/10556/4592
Title: OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences
Authors: Coppola, Antonietta
Krithika, Sundararaman
Iacomino, Michele
Balestrini, Simona
Hernandez-Hernandez, Laura
Meletti, Stefano
Gobbi, Giuseppe
Ferlazzo, Edoardo
Giordano, Lucio
Casellato, Susanna
Sofia, Vito
Striano, Pasquale
Bilo, Leonilda
Nigro, Vincenzo
Torella, Annalaura
Musacchia, Francesco
Zara, Federico
Sisodiya, Sanjay M.
Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples>
Issue Date: 2019
Citation: Coppola A, Krithika S, Iacomino M, Balestrini S, Hernandez-Hernandez L, Meletti S, Gobbi G, Ferlazzo E, Giordano L, Casellato S, Sofia V, Striano P, Bilo L, Nigro V, Torella A, Musacchia F, Zara F, Sisodiya SM. OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences. [oral communications presentata a: 8th Annual Meeting of the Neapolitan Brain Group, Naples, 13 December 2018]. Translational Medicine @ UniSa. Volume Special Issue 1(2019): 5.
URI: http://www.translationalmedicine.unisa.it/index
http://elea.unisa.it:8080/xmlui/handle/10556/4592
http://dx.doi.org/10.14273/unisa-2786
ISSN: 2239-9747
Appears in Collections:Translational Medicine @ UniSa. Volume Special Issue 01 2019

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