Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Arthur J. Barela"'
Autor:
Alan L. Goldin, Frank G. Lin, Ligia A. Papale, Robert C. Liu, Karoni Dutt, Anupama Shankar, Andrew Escayg, Christopher D. Makinson, Arthur J. Barela
Publikováno v:
Makinson, CD; Dutt, K; Lin, F; Papale, LA; Shankar, A; Barela, AJ; et al.(2016). An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior. Experimental Neurology, 275, 46-58. doi: 10.1016/j.expneurol.2015.09.008. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/11t2366n
Experimental neurology, vol 275 Pt 1, iss 0 1
Experimental neurology, vol 275 Pt 1, iss 0 1
© 2015 Elsevier Inc. Understanding the role of SCN8A in epilepsy and behavior is critical in light of recently identified human SCN8A epilepsy mutations. We have previously demonstrated that Scn8amedand Scn8amed-jomice carrying mutations in the Scn8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a59eeae6b4a2e060db2ef33184cc1609
https://escholarship.org/uc/item/11t2366n
https://escholarship.org/uc/item/11t2366n
Autor:
Salina P. Waddy, Andrew Escayg, Aimee Anido, Arthur J. Barela, Jessica Ezzell Hunter, Sandra L. Helmers, Alan L. Goldin, Jay G. Lickfett
Publikováno v:
The Journal of Neuroscience. 26:2714-2723
Mutations in three voltage-gated sodium channel genes,SCN1A,SCN2A, andSCN1B, and two GABAAreceptor subunit genes,GABRG2andGABRD, have been identified in families with generalized epilepsy with febrile seizures plus (GEFS+). A novel mutation, R859C, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5462bc94f36522397b6895289154b75
https://doi.org/10.1523/jneurosci.2977-05.2006
https://doi.org/10.1523/jneurosci.2977-05.2006
