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pro vyhledávání: '"Chantel Trager"'
Autor:
Donald P. Younkin, Christopher A. Reid, Carol J. Milligan, Dennis J. Dlugos, Chantel Trager, Melody Li, Steven Petrou, Sarah E. Heron, Anu Venkat, Umesh Nair, Samuel F. Berkovic, Ingrid E. Scheffer, Slavé Petrovski, David Goldstein, Elena V. Gazina, Leanne M. Dibbens
Publikováno v:
Annals of Neurology. 75:581-590
Objective Mutations in KCNT1 have been implicated in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) and epilepsy of infancy with migrating focal seizures (EIMFS). More recently, a whole exome sequencing study of epileptic encephalopathie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d74c9ff6bd7ec82348498d0e80683978
https://doi.org/10.1002/ana.24128
https://doi.org/10.1002/ana.24128
