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

[Gene detection of GPD1-L and the association with sudden unexplained death syndrome in young adults].

Fa yi xue za zhi - 1 Oct 2013

Xu Xiao-long, Wang Wen, Liu Chao, Hou Yi-ding, Huang Lei, Liu Chang-hui, Li Yue, Cheng Jian-ding

Abstract excerpt

OBJECTIVE: To analyze the variations of glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) and address the association with sudden manhood death syndrome (SMDS). METHODS: The genomic DNA was extracted from blood samples of the SMDS group and the normal control group. The exons, exon-intron boundaries and 3'-UTRs of coding region of GPD1-L were PCR amplified and DNA sequenced directly to confirm the types of...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Death, Sudden

Share to DNA Mutational Analysis

Share to DNA Primers

Share to Glycerolphosphate Dehydrogenase

Share to Young Adult

Source

Identifiers

PMID: 24466774

Genes

GPD1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

[Gene detection of GPD1-L and the association with sudden unexplained death syndrome in young adults].PMID 24466774Read ↗

Whole-exome sequencing identifies a novel mutation of GPD1L (R189X) associated with familial conduction disease and sudden death.Semantic proximity Read ↗

Clinical characteristics and variant analyses of transient infantile hypertriglyceridemia related to GPD1 geneSemantic proximity Read ↗

Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.Semantic proximity Read ↗

A very rare cause of hypertrygliseridemia in infancy: a novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene.Semantic proximity Read ↗

Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome.Semantic proximity Read ↗

[KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].Semantic proximity Read ↗

[A case of transient infantile hypertriglyceridemia caused by mutations in the glycerol-3-phosphate dehydrogenase 1 gene].Semantic proximity Read ↗

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case reportSemantic proximity Read ↗

[Distribution of erythrocyte EsD and PGM1 (phosphoglucomutase) phenotypes in the Han population of Changsha district].Semantic proximity Read ↗

GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A.Semantic proximity Read ↗

[Correlation of NOS1AP gene polymorphisms with sudden unexpected death in Chinese Han population].Semantic proximity Read ↗

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