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Article

Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Jan 2006

Hering Robert, Frade-Martinez Rosario, Bajanowski Thomas, Poets Christian F, Tschentscher Frank, Riess Olaf

Abstract excerpt

BACKGROUND: Sudden infant death syndrome (SIDS) constitutes the most frequent cause of death in the postperinatal period in Germany. Recently, a lethal phenotype characterized by sudden infant death with dysgenesis of the testes syndrome (SIDDT) was identified to be caused by loss of function mutations in the TSPYL1 gene. PURPOSE: The study's purpose was to reveal a possible role of TSPYL1 in SIDS. METHODS: DNA...

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Source

Identifiers

PMID: 16418600
DOI: 10.1097/01.gim.0000195898.15290.03

Genes

TSPYL1

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.

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Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.PMID 16418600Read ↗

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