Publication | Open Access

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene

Developmental AnomalyUrologyMendelian DisorderUrinary TractWhole-exome SequencingGeneticsMedicineGenetic DisorderNew Causative GeneDisease Gene IdentificationGenomicsMolecular DiagnosticsSequencingNephrology