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

• Main Authors: Meredith Harris (Author), Meredith P. Schuh (Author), David McKinney (Author), Kenneth Kaufman (Author), Elif Erkan (Author)
• Formato: Livro
• Publicado em: Frontiers Media S.A., 2022-08-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

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...