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pro vyhledávání: '"Stefania Beratta"'
Autor:
Chiara Verpelli, Stefania Beratta, Luisa Ponzoni, Carlo Sala, Mariaelvina Sala, Laura Gritti, Paolo Scalmani, Massimo Mantegazza
Publikováno v:
Molecular Autism
Molecular Autism, Vol 13, Iss 1, Pp 1-22 (2022)
Molecular Autism, Vol 13, Iss 1, Pp 1-22 (2022)
Background Dravet Syndrome is a severe childhood pharmaco-resistant epileptic disorder mainly caused by mutations in the SCN1A gene, which encodes for the α1 subunit of the type I voltage-gated sodium channel (NaV1.1), that causes imbalance between