Lumasiran for primary hyperoxaluria type 1: What we have learned?
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DOI: 10.3389/fped.2022.1052625
Abstract: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive genetic disorder caused by mutations in the AGXT gene. The hepatic peroxisomal enzyme alanine glyoxylate aminotransferase (AGT) defects encoded by the AGXT gene increase oxalate… read more here.
Keywords: primary hyperoxaluria; treatment ph1; hyperoxaluria type; ph1 ... See more keywords