Article

Identification of Arrhythmia-Associated Gene Mutations in Chinese Patients with Primary Electrical Disorders or Sudden Cardiac Death

2024-01-01

Abstract excerpt

Background: Sudden cardiac death (SCD), unexpected death based on sudden cardiac ejection cessation, accounts for 15–20% of unnatural deaths in developed countries. Primary electrical disorders (PEDs), a group of cardiac rhythm abnormalities without detectable structural heart disease, are a major cause of SCD in people younger than 35 years of age. Cardiac muscle contraction and relaxation are triggered by the ac...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 310a0e60-909b-59c9-b2a8-72c8763ad5e8
DOI: 10.15212/cvia.2024.0018

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Identification of Arrhythmia-Associated Gene Mutations in Chinese Patients with Primary Electrical Disorders or Sudden Cardiac DeathDOI 10.15212/cvia.2024.0018Read

Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia.Semantic proximity Read

Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.Semantic proximity Read

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function.Semantic proximity Read

Molecular and genetic basis of sudden cardiac deathSemantic proximity Read

Ion Channel Disorders and Sudden Cardiac Death.Semantic proximity Read

Identification of Genetic Variants in Patients with Idiopathic Ventricular Arrhythmia by Taiwan Arrhythmia Gene Panel Implying Underlying MechanismsSemantic proximity Read

Genetics of sudden cardiac death.Semantic proximity Read

Genetics of sudden cardiac death syndromes.Semantic proximity Read

Whole exome sequencing with a focus on cardiac disease-associated genes in families of sudden unexplained deaths in Yunnan, southwest of China.Semantic proximity Read

Sudden cardiac death and inherited arrhythmia syndromes.Semantic proximity Read

Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death.Semantic proximity Read

Genetic predisposition to sudden cardiac death.Semantic proximity Read