Concepedia

Recurrent intrauterine fetal loss due to near absence of HERG: Clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation

Zahurul A. Bhuiyan, Tarek Momenah, Qiuming Gong, Ahmad S. Amin, Saleh Al Ghamdi, J. S. Carvalho, Tessa Homfray, Marcel M. A. M. Mannens, Zhengfeng Zhou, Arthur A.M. Wilde

Heart Rhythm · 2008 · 63 citations · 25 references

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25

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

Mark Curran, Igor Splawski, Katherine W. Timothy et al. · Cell · 1995 · 2.3K citations · Full text

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Prevalence of the Congenital Long-QT Syndrome

Peter J. Schwartz, Marco Stramba‐Badiale, Lia Crotti et al. · Circulation · 2009 · 1.1K citations

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Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.

Michael C. Sanguinetti, Mark Curran, Peter Spector et al. · Proceedings of the National Academy of Sciences · 1996 · 473 citations

, , +17

Drugs That Induce Repolarization Abnormalities Cause Bradycardia in Zebrafish

David J. Milan, Travis A. Peterson, Jeremy N. Ruskin et al. · Circulation · 2003 · 440 citations · Full text

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Most LQT2 Mutations Reduce Kv11.1 (hERG) Current by a Class 2 (Trafficking-Deficient) Mechanism

Corey L. Anderson, Brian P. Delisle, Blake D. Anson et al. · Circulation · 2006 · 417 citations

, , +17