Evidence map›Paper›PMID 39962939›Full record

ArticleJournal of Korean medical science2025

Identification of Mutations of the

Min-Jeong Son, Min-Kyoung Kim, Seong Ho Yoo

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Min-Jeong SonDepartment of Forensic Medicine and Institute of Forensic Medicine, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8225-8328
Min-Kyoung KimDivision of Forensic Medicine, National Forensic Service, Seoul, Korea.ORCID https://orcid.org/0000-0003-0291-8512
Seong Ho YooDepartment of Forensic Medicine and Institute of Forensic Medicine, Seoul National University College of Medicine, Seoul, Korea. yoosh@snu.ac.kr.ORCID https://orcid.org/0000-0001-5294-0596

Funding

Ministry of the EducationMinistry of the Interior and Safety 800-20160361National Forensic Service 2015-forensic medicine-05
6 · The paper itself

Abstract

backgroundDespite efforts by the National Education on Sleeping Environment to reduce sudden infant death syndrome (SIDS), it remains the leading cause of post-neonatal mortality. In Korea, the incidence of SIDS was estimated at 0.4 per 1,000 infants in 2022. Mutations in the ryanodine receptor 2 (

methodsWe extracted DNA from archived formalin-fixed, paraffin-embedded myocardial tissues from 249 SIDS cases autopsied between 2005 and 2017. DNA analysis focused on sequencing key exons (3, 8, 14, 15, 37, 42, 44-47, 49, 50, 83, 87-91, 93-95, 97, 99, and 100-105) of the

resultsAmong the 249 SIDS cases, 62% were male infants, with an average age of 124 days, all of Asian-Korean descent. We identified two previously unreported

conclusionOur study identified two

Indexed as

MutationRyanodine Receptor Calcium Release ChannelSudden Infant DeathExonsFemaleHumansInfantInfant, NewbornMaleRepublic of KoreaRyanodine Receptor Calcium Release ChannelRyR2 protein, humanCatecholaminergic Polymorphic Ventricular Tachycardia (CPVT)Gene MutationMolecular AutopsyRyanodine Receptor 2 (RYR2)Sudden Infant Death Syndrome

Identifiers

PMID39962939
PMCPMC11832885

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.