Phenotypic Spectrum of HCN4 Mutations-Reference-Cited by-同舟云学术

Phenotypic Spectrum of HCN4 Mutations

Published:2018-02 Issue:2 Volume:11 Page:
ISSN:2574-8300
Container-title:Circulation: Genomic and Precision Medicine
language:en
Short-container-title:Circ Genom Precis Med.

Author:

Servatius Helge¹,Porro Alessandro¹,Pless Stephan A.¹,Schaller André¹,Asatryan Babken¹,Tanner Hildegard¹,de Marchi Stefano F.¹,Roten Laurent¹,Seiler Jens¹,Haeberlin Andreas¹,Baldinger Samuel H.¹,Noti Fabian¹,Lam Anna¹,Fuhrer Juerg¹,Moroni Anna¹,Medeiros-Domingo Argelia¹

Affiliation:

1. From the Department of Cardiology (H.S., B.A., H.T., S.F.d.M., L.R., J.S., A.H., S.H.B., F.N., A.L., J.F., A.M.-D.) and Division of Human Genetics, Department of Pediatrics (A.S.), Inselspital, Bern University Hospital, University of Bern, Switzerland; Artificial Organ Center for Biomedical Engineering Research, University of Bern, Switzerland (A.H.); Department of Biosciences, CNR IBF-Milano, Università degli Studi di Milano, Italy (A.P., A.M.); and Department of Drug Design and Pharmacology,...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference28 articles.

1. Heteromeric HCN1–HCN4 Channels: A Comparison with Native Pacemaker Channels from the Rabbit Sinoatrial Node

2. The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart

3. A family of hyperpolarization-activated mammalian cation channels

4. Proteolytic Processing of HCN2 and Co-assembly with HCN4 in the Generation of Cardiac Pacemaker Channels

5. Functional Characterization of a Trafficking-defective HCN4 Mutation, D553N, Associated with Cardiac Arrhythmia

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