Whole Exome Sequencing Reveals Promising Genes Associated with Congenital Renal Parenchymal Anomalies in Greek Children

Background: Congenital anomalies of the kidney and urinary tract (CAKUT) comprise a broad spectrum of malformations and constitute the leading cause of end-stage kidney disease (ESKD) in childhood. Despite extensive research, a monogenic cause is identified in only ~10% of cases, while variable pene...

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Egile Nagusiak:	Anna Zisi, Charilaos Kostoulas, Athanasia Sesse, Chrysoula Kosmeri, Anastasios Serbis, Hane Lee, Ioannis Georgiou, Ekaterini Siomou
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	MDPI AG 2026-05-01
Saila:	Children
Gaiak:	CAKUT children variants genes whole exome sequencing
Sarrera elektronikoa:	https://www.mdpi.com/2227-9067/13/6/752
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