A Novel Somatic Variant in HEY2 Unveils an Alternative Splicing Isoform Linked to Ventricular Septal Defect
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DOI: 10.1007/s00246-019-02099-y
Abstract: Congenital heart defects (CHDs) are the leading cause of death in infants under 1 year of age. Aberrations in the expression and function of cardiac transcription factors (TFs) are a major contributor to CHDs. Despite the… read more here.
Keywords: hey2; novel somatic; ventricular septal; variant hey2 ... See more keywords