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pro vyhledávání: '"Senad, KOLAR"'
Autor:
Katarina, Ceska, Pavlina, Danhofer, Ondrej, Horak, Klara, Spanelova, Senad, Kolar, Hana, Oslejskova, Stefania, Aulicka
Publikováno v:
Bratislava Medical Journal. 123:483-486
with the Dravet's syndrome phenotype are associated with the detection of a sequence variant in the SCN1A gene (alpha 1 subunit of the voltage-gated sodium channel) (2). However, sequence variants in the SCN1A gene are associated with a very broad cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68aa01a0d058f2f3ff4660f3670cf6e4
https://doi.org/10.4149/bll_2022_076
https://doi.org/10.4149/bll_2022_076
