Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction

Abstract

Mutations in TSHZ2 and TSHZ3 are not a major cause of PUJO, at least in Albanian and Macedonian populations. Expression of these genes in the human fetal ureter emphasizes the importance of analysing these genes in other groups of patients with renal tract malformations.