HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients

摘要

Primary hyperoxaluria type 3 ( 3) is due to mutations in the recently identified 4‐hydroxy‐2‐oxoglutarate aldolase ( ) gene. 3 might be the least severe form with a milder phenotype with good preservation of kidney function in most patients. The aim of this study was to report three 3 cases carrying mutations in .