Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary Tract

• Asıl Yazarlar: Meredith Harris (Yazar), Meredith P. Schuh (Yazar), David McKinney (Yazar), Kenneth Kaufman (Yazar), Elif Erkan (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Frontiers Media S.A., 2022-08-01T00:00:00Z.
• Konular: article
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Fetal and neonatal interventions (e.g., amnioinfusions, amniotic shunting, and infant dialysis) have increased survival of infants with severe Congenital Anomalies of the Kidney and Urinary Tract (CAKUT), however, outcomes vary dramatically. Our aim was to perform Whole Exome Sequencing (WES) in a u...