High-throughput genetic characterization of a cohort of Brugada syndrome patients-Reference-Cited by-同舟云学术

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High-throughput genetic characterization of a cohort of Brugada syndrome patients

Published:2015-07-28 Issue:20 Volume:24 Page:5828-5835
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Di Resta Chiara,Pietrelli Alessandro,Sala Simone,Della Bella Paolo,De Bellis Gianluca,Ferrari Maurizio,Bordoni Roberta,Benedetti Sara

Funder

NEDD

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/20/5828/13926903/ddv302.pdf

Reference33 articles.

1. Brugada Syndrome: Report of the Second Consensus Conference

2. Genetic testing for inherited cardiac disease

3. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome

4. An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

5. KCNE1 divides the voltage sensor movement in KCNQ1/KCNE1 channels into two steps;Barro-Soria;Nat. Commun.,2014

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1. Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel;Orphanet Journal of Rare Diseases;2022-10-27

2. Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?;Genes;2022-09-28

3. The Genetics of Brugada Syndrome;Annual Review of Genomics and Human Genetics;2022-08-31

4. Recent Progress in Drug Repurposing Using Protein Variants and Amino Acids in Disease Phenotypes/Disorders;Drug Repurposing - Molecular Aspects and Therapeutic Applications;2022-06-01

5. Genomic and Non-Genomic Regulatory Mechanisms of the Cardiac Sodium Channel in Cardiac Arrhythmias;International Journal of Molecular Sciences;2022-01-26

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