Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection

Number of the records: 1

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

Number of the records: 1