Concepedia

A family with Andersen-Tawil syndrome and dilated cardiomyopathy

B. A. Schoonderwoerd, Ans C.P. Wiesfeld, Arthur A.M. Wilde, Freek van den Heuvel, J. Peter van Tintelen, Maarten P. van den Berg, Dirk J. van Veldhuisen, Isabelle C Van Gelder

Heart Rhythm · 2006 · 33 citations · 31 references

DOI

Concepts

References

31

Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

Diane Fatkin, Calum A. MacRae, Takeshi Sasaki et al. · New England Journal of Medicine · 1999 · 1.4K citations · Full text

, , +17

Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi et al. · Cell · 2001 · 998 citations · Full text

, , +14

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Natascia Tiso · Human Molecular Genetics · 2001 · 806 citations · Full text

, , +17

Alterations of K+ currents in isolated human ventricular myocytes from patients with terminal heart failure.

D J Beuckelmann, Michael Näbauer, Erland Erdmann · Circulation Research · 1993 · 735 citations · Full text

, , +17

Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban

Joachim P. Schmitt, Mitsuhiro Kamisago, Michio Asahi et al. · Science · 2003 · 628 citations

, , +15