Associated Papers
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias.
Brandão KO et al.
Stem Cell Reports, 2020
33176122 (PubMed )
Supplement: mmc2.xlsx › Supplementary_table_4
Mutation analysis of candidate genes SCN1B, KCND3 and ANK2 in patients with clinical diagnosis of long QT syndrome.
Raudenská M et al.
Physiological Research, 2008
[Mutational analysis of LQT genes in individuals with drug induced QT interval prolongation].
Novotný T et al.
Vnitrni Lekarstvi, 2006
[The role of ergometric testing in diagnosis of latent long QT syndrome].
Novotný T et al.
Vnitrni Lekarstvi, 2000
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