The Symptom Complex of Familial Sinus Node Dysfunction and Myocardial Noncompaction Is Associated With Mutations in the HCN4 Channel-Reference-Cited by-同舟云学术

The Symptom Complex of Familial Sinus Node Dysfunction and Myocardial Noncompaction Is Associated With Mutations in the HCN4 Channel

Published:2014-08 Issue:8 Volume:64 Page:757-767
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:

Schweizer Patrick A.,Schröter Julian,Greiner Sebastian,Haas Jan,Yampolsky Pessah,Mereles Derliz,Buss Sebastian J.,Seyler Claudia,Bruehl Claus,Draguhn Andreas,Koenen Michael,Meder Benjamin,Katus Hugo A.,Thomas Dierk

Funder

Max-Planck-Society

German Cardiac Society

Medical Faculty of the University of Heidelberg

Hengstberger Foundation

Joachim Siebeneicher Foundation

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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3. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy;Luxán;Nat Med,2013

4. Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations;Hermida-Prieto;Am J Cardiol,2004

5. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction;Vatta;J Am Coll Cardiol,2003

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