Article
Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome Sequencing
2023-09-12
Abstract excerpt
<h4>Purpose</h4> To gain insights into potential genetic factors contributing to the infant’s vulnerability to Sudden Unexpected Infant Death (SUID). <h4>Methods</h4> Whole Genome Sequencing (WGS) was performed on 145 infants that succumbed to SUID, and 576 healthy adults. Variants were filtered by gnomAD allele frequencies and predictions of functional consequences. <h4>Results</h4> Variants of interest were iden...
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Identifiers and source
- Literature Corpus work
- 127644fb-bec0-55c7-a892-632bd6597309
- DOI
- 10.1101/2023.09.11.23295207
