HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy-Reference-Cited by-同舟云学术

HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy

Published:2014-08 Issue:8 Volume:64 Page:745-756
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

Milano Annalisa,Vermeer Alexa M.C.,Lodder Elisabeth M.,Barc Julien,Verkerk Arie O.,Postma Alex V.,van der Bilt Ivo A.C.,Baars Marieke J.H.,van Haelst Paul L.,Caliskan Kadir,Hoedemaekers Yvonne M.,Le Scouarnec Solena,Redon Richard,Pinto Yigal M.,Christiaans Imke,Wilde Arthur A.,Bezzina Connie R.

Funder

Netherlands Heart Foundation

Netherlands Heart Institute

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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3. A novel mutation in the HCN4 gene causes symptomatic sinus bradycardia in Moroccan Jews;Laish-Farkash;J Cardiovasc Electrophysiol,2010

4. Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia;Nof;Circulation,2007

5. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene SCN5A;Benson;J Clin Invest,2003

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