Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome-Reference-Cited by-同舟云学术

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome

Published:2015-03 Issue: Volume:80 Page:186-195
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Wemhöner Konstantin,Friedrich Corinna,Stallmeyer Birgit,Coffey Alison J.,Grace Andrew,Zumhagen Sven,Seebohm Guiscard,Ortiz-Bonnin Beatriz,Rinné Susanne,Sachse Frank B.,Schulze-Bahr Eric,Decher Niels

Funder

Deutsche Forschungsgemeinschaft

IMF

Fondation Leducq

Nora Eccles Treadwell Foundation

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

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4. Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel;Mikami;Nature,1989

5. Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart;Schultz;Proc Natl Acad Sci U S A,1993

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