Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing-Reference-Cited by-同舟云学术

Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing

Published:2022-05 Issue:5 Volume:19 Page:798-806
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Novelli Valeria^ORCID,Memmi Mirella,Malovini Alberto,Mazzanti Andrea,Liu Nian,Yanfei Ruan,Bongianino Rossana,Denegri Marco,Monteforte Nicola,Bloise Raffaella,Morini Massimo,Napolitano Carlo^ORCID

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference24 articles.

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3. Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing;Crotti;J Am Coll Cardiol,2012

4. L-type calcium channel mutations in Japanese patients with inherited arrhythmias;Fukuyama;Circ J,2013

5. Reappraisal of reported genes for sudden arrhythmic death: evidence-based evaluation of gene validity for Brugada syndrome;Hosseini;Circulation,2018

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1. Inherited channelopathies and acquired phenocopies;Genomic and Molecular Cardiovascular Medicine;2024

2. SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern;Journal of Cardiovascular Medicine;2023-10-31

3. Brugada Syndrome: More than a Monogenic Channelopathy;Biomedicines;2023-08-18

4. Genetics of sinoatrial node function and heart rate disorders;Disease Models & Mechanisms;2023-05-01

5. Functional identification of hot-spot mutations in cardiac calcium channel genes associated with the J wave syndromes;Philosophical Transactions of the Royal Society B: Biological Sciences;2023-05