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	1.	Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome. [electronic resource] by Raudenská, M Bittnerová, A Novotný, T Floriánová, A Chroust, K Gaillyová, R Semrád, B Kadlecová, J Šišáková, M Toman, O Spinar, J Producer: 20090305 In: Physiological research vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Mutational analysis of LQT genes in individuals with drug induced QT interval prolongation]. [electronic resource] by Novotný, T Kadlecová, J Papousek, I Chroust, K Bittnerová, A Floriánová, A Cesková, E Weislamplová, M Pálenský, V Sisáková, M Toman, O Gaillyová, R Spinar, J Producer: 20060523 In: Vnitrni lekarstvi vol. 52 Availability: No items available. Save to lists Add to cart (remove)

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