Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
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Familial vesicoureteral reflux 3

Familial vesicoureteral reflux 3 is an autosomal dominant disorder caused by mutations of the SOX17 gene.

Systematic

Vesicoureteral reflux
Familial vesicoureteral reflux 2
Familial vesicoureteral reflux 3
SOX17
Familial vesicoureteral reflux 8

References:

1.

Gimelli S et al. (2010) Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract.

external link
2.

OMIM.ORG article

Omim 613674 external link
Update: Aug. 14, 2020
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