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

PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population.

International journal of legal medicine - 1 Jul 2014

Liebrechts-Akkerman Germaine, Liu Fan, Lao Oscar, Ooms Ariadne H A G, van Duijn Kate, Vermeulen Mark, Jaddoe Vincent W, Hofman Albert, Engelberts Adèle C, Kayser Manfred

Abstract excerpt

Unclassified sudden infant death (USID) is the sudden and unexpected death of an infant that remains unexplained after thorough case investigation including performance of a complete autopsy and review of the circumstances of death and the clinical history. When the infant is below 1 year of age...

Read the complete abstract on PubMed

Topics

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

Share to Exons
Share to Homeodomain Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Netherlands

Share to Peptides

Share to Repetitive Sequences, Nucleic Acid

Share to Sudden Infant Death

Share to Transcription Factors

Source

Identifiers

PMID: 24442913
DOI: 10.1007/s00414-013-0962-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24442913-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population.PMID 24442913Read ↗

Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.Semantic proximity Read ↗

A Common 3′UTR Variant of the PHOX2B Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian PopulationSemantic proximity Read ↗

That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS).Semantic proximity Read ↗

Causative and common PHOX2B variants define a broad phenotypic spectrumSemantic proximity Read ↗

Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases.Semantic proximity Read ↗

Gene variants predisposing to SIDS: current knowledge.Semantic proximity Read ↗

Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit.Semantic proximity Read ↗

Sudden infant death syndrome: another year of new hope but no cure.Semantic proximity Read ↗

Sudden Infant Death Syndrome: review of implicated genetic factors.Semantic proximity Read ↗

HTR2A variation and sudden infant death syndrome: a case-control analysis.Semantic proximity Read ↗

Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene.Semantic proximity Read ↗

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.Semantic proximity Read ↗

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