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Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection
Title Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection Author Surový Milan Co-authors Šoltýsová Andrea 1980- SAVUKTRA ; SAVBIOMED - Ústav klinického a translačného výskumu BMC SAV Kolnikova M. Sýkora Pavol Ilenčíková Denisa Ficek Andrej Radvánszky Ján 1982- SAVUKTRA ; SAVBIOMED - Ústav klinického a translačného výskumu BMC SAV Kádaši Ľudevít 1952- SAVUKTRA ; SAVBIOMED - Ústav klinického a translačného výskumu BMC SAV ORCID Source document General Physiology and Biophysics. Vol. 35, no. 3 (2016), p. 333-342 Language eng - English Document kind rozpis článkov z periodík (rbx) Citations LAMAR, Tyra - VANOYE, Carlos G. - CALHOUN, Jeffrey - WONG, Jennifer C. - DUTTON, Stacey B. B. - JORGE, Benjamin S. - VELINOV, Milen - ESCAYG, Andrew - KEARNEY, Jennifer A. SCN3A deficiency associated with increased seizure susceptibility. In NEUROBIOLOGY OF DISEASE. ISSN 0969-9961, 2017, vol. 102, no., pp. 38-48. Category ADDA - Scientific papers in domestic journals registered in Current Contents Connect with IF (impacted) Category of document (from 2022) V3 - Vedecký výstup publikačnej činnosti z časopisu Type of document článok Year 2016 Registered in WOS Registered in SCOPUS Registered in CCC DOI 10.4149/gpb_2016002 article
File name Access Size Downloaded Type License Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection.pdf available 254.1 KB 0 Publisher's version rok CC IF IF Q (best) JCR Av Jour IF Perc SJR SJR Q (best) CiteScore A rok vydania rok metriky IF IF Q (best) SJR SJR Q (best) 2016 2015 0.892 Q4 0.387 Q3
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