Identification of Decreased Butyrylcholinesterase in Sudden Infant Death Syndrome Is, at Best, a First Step Toward Preventive Screening
Author:
Affiliation:
1. Department of Laboratory Medicine and Pathology, Mayo Clinic , Rochester, MN
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
https://academic.oup.com/clinchem/article-pdf/69/2/116/49033704/hvac134.pdf
Reference5 articles.
1. Butyrylcholinesterase is a potential biomarker for sudden infant death syndrome;Harrington;EBioMedicine,2022
2. Heart rate variability analysis to evaluate autonomic nervous system maturation in Neonates: an expert opinion;Patural;Front Pediatr,2022
3. Explaining sudden infant death with cardiac arrhythmias: complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants;Liebrechts-Akkerman;Forensic Sci Int Genet,2020
4. Only halfway there with sudden infant death syndrome;Goldstein;N Engl J Med,2022
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