Analysis of SCN5A Gene Variants in East Slovak Patients with Cardiomyopathy. (Q39460292)

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21 March 2020

title

Analysis of SCN5A Gene Variants in East Slovak Patients with Cardiomyopathy (English)

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21 March 2020

author name string

Mariana Priganc

1

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21 March 2020

Michaela Zigová

2

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21 March 2020

Iveta Boroňová

3

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21 March 2020

Jarmila Bernasovská

4

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21 March 2020

Dana Dojčáková

5

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21 March 2020

Viktória Szabadosová

6

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21 March 2020

Marta Mydlárová Blaščáková

7

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21 March 2020

Iveta Tóthová

8

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21 March 2020

Ján Kmec

9

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21 March 2020

Ivan Bernasovský

10

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21 March 2020

language of work or name

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24 August 2016

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Journal of Clinical Laboratory Analysis

21 March 2020

published in

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21 March 2020

volume

31

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21 March 2020

issue

2

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Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

21 March 2020

cites work

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Association of fibrosis with mortality and sudden cardiac death in patients with nonischemic dilated cardiomyopathy

21 January 2018

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The genetic landscape of cardiomyopathy and its role in heart failure.

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A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome

21 January 2018

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Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: the Jackson Heart Study

21 January 2018

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21 January 2018

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Defining the disconnect between in vitro models and human arrhythmogenic disease: context matters

21 January 2018

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Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects

21 January 2018

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Inherited disorders of voltage-gated sodium channels

21 January 2018

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Brugada syndrome: recent advances and controversies.

21 January 2018

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SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism

21 January 2018

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A Proton Leak Current through the Cardiac Sodium Channel Is Linked to Mixed Arrhythmia and the Dilated Cardiomyopathy Phenotype

21 January 2018

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Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

21 January 2018

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21 January 2018

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21 January 2018

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Molecular and clinical characterization of a novel SCN5A mutation associated with atrioventricular block and dilated cardiomyopathy

21 January 2018

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A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese?

21 January 2018

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Contrast-Enhanced Ultrasonography Features of Breast Malignancies with Different Sizes: Correlation with Prognostic Factors

21 January 2018

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Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome.

21 January 2018

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

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Nav 1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link?

21 January 2018

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Risk of sudden death and outcome in patients with hypertrophic cardiomyopathy with benign presentation and without risk factors

21 January 2018

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Targeted Next-Generation Sequencing Reveals Hot Spots and Doubly Heterozygous Mutations in Chinese Patients with Familial Cardiomyopathy

21 January 2018

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PubMed

12 December 2020

SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

1 reference

PubMed

12 December 2020

Dilated cardiomyopathy due to sodium channel dysfunction: what is the connection?

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PubMed

12 December 2020

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12 December 2020

Identifiers

DOI

10.1002/JCLA.22037

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27554632 AND SRC:MED&resulttype=core&format=json

21 March 2020

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21 March 2020

PubMed publication ID

27554632

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