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Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

8 Aug 2022

Abstract excerpt

Congenital heart disease (CHD) is the most frequent kind of birth deformity in human beings and the leading cause of neonatal mortality worldwide. Although genetic etiologies encompassing aneuploidy, copy number variations, and mutations in over 100 genes have been uncovered to be involved in the pathogenesis of CHD, the genetic components predisposing to CHD in most cases remain unclear. We recruited a family...

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PMID: 36010266
DOI: 10.3390/diagnostics12081917

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Identification of SOX18 as a New Gene Predisposing to Congenital Heart DiseasePMID 36010266Read ↗

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