Epigenome-wide association study for sudden unexpected infant death
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DOI: 10.1016/j.fsigss.2019.10.188
Abstract: Abstract Many genomic variants associated with sudden unexpected death (SUD) have been found with the use of the next generation sequencing (NGS), and registered in the clinical pathogenetic variant databases such as SIFT, Poly-Phen2 and… read more here.
Keywords: methylation; sid cases; infant death; unexpected infant ... See more keywords