Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage–Dependent L-Type Calcium Channel-Reference-Cited by-同舟云学术

Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage–Dependent L-Type Calcium Channel

Published:2011-03-04 Issue:5 Volume:108 Page:607-618
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circ Res

Author:

Napolitano Carlo¹,Antzelevitch Charles¹

Affiliation:

1. From the Molecular Cardiology Laboratories (C.N.), IRCCS Salvatore Maugeri Foundation, Pavia, Italy; Cardiovascular Genetics (C.A.), Leon Charney Division of Cardiology, New York University; and Masonic Medical Research Laboratory (C.A.), Utica, NY.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference96 articles.

1. Novel functional properties of Ca2+channel β subunits revealed by their expression in adult rat heart cells

2. Ca 2+ Influx–Induced Sarcoplasmic Reticulum Ca 2+ Overload Causes Mitochondrial-Dependent Apoptosis in Ventricular Myocytes

3. The electrical properties of crustacean muscle fibres

4. History of calcium antagonists;Fleckenstein A;Circ Res,1983

5. Bradycardia and Slowing of the Atrioventricular Conduction in Mice Lacking Ca V 3.1/α 1G T-Type Calcium Channels

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