Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.

Forensic science international - 1 Feb 2014

Huang Lei, Liu Chao, Tang Shuangbo, Su Terry, Cheng Jianding

Abstract excerpt

To investigate the genetic variants of the RyR2 gene in sudden unexplained nocturnal death syndrome (SUNDS) in the southern Chinese Han population, we genetically screened 29 of the 105 coding exons of the RyR2 gene associated with catecholaminergic polymorphic ventricular tachycardia (CPVT) and arrhythmogenic right ventricular cardiomyopathy (ARVC) in sporadic SUNDS victims using polymerase chain reaction (PCR)...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to China
Share to Death, Sudden
Share to Ethnicity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forensic Genetics

Share to Ryanodine Receptor Calcium Release Channel

Share to Sequence Analysis

Share to Young Adult

Source

Identifiers

PMID: 24447446
DOI: 10.1016/j.forsciint.2013.12.007

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.PMID 24447446Read ↗

Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases.Semantic proximity Read ↗

Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.Semantic proximity Read ↗

Molecular pathological study on LRRC10 in sudden unexplained nocturnal death syndrome in the Chinese Han population.Semantic proximity Read ↗

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

Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.Semantic proximity Read ↗

Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?Semantic proximity Read ↗

GJA1 gene variations in sudden unexplained nocturnal death syndrome in the Chinese Han population.Semantic proximity Read ↗

Sudden unexplained nocturnal death syndrome in Southern China: an epidemiological survey and SCN5A gene screening.Semantic proximity Read ↗

Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.Semantic proximity Read ↗

Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population.Semantic proximity Read ↗

Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China.Semantic proximity Read ↗

Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.