NOTCH1 & Heart Defects: New Genetic Insights
A breakthrough in genetic diagnostics offers new hope for families grappling with the uncertainty of congenital heart defects (CHDs), a condition affecting roughly 1-2% of newborns. Researchers at the University Medicine Oldenburg in Germany have developed a novel method to pinpoint whether variations in the NOTCH1 gene are the causative factor in these defects, moving … Read more