Associated Papers
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health records.
Akawi N et al.
Frontiers in Molecular Biosciences, 2024
39411402 (PubMed )
Supplement: Table1.XLSX › Supplemental_Table_S11
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
Select a paper to view details