HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.


BACKGROUND Primary hyperoxaluria type 3 (PH3) is due to mutations in the recently identified 4-hydroxy-2-oxoglutarate aldolase (HOGA1) gene. PH3 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 PH3 cases carrying mutations in HOGA1. MATERIALS AND… (More)
DOI: 10.1002/jcla.22053


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