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Published in 2021 at "Kidney International Reports"
DOI: 10.1016/j.ekir.2021.01.029
Abstract: Introduction Primary hyperoxaluria (PH) is a family of 3 rare genetic disorders of hepatic glyoxylate metabolism that lead to overproduction and increased renal excretion of oxalate resulting in progressive renal damage. LDHA inhibition of glyoxylate-to-oxalate…
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Keywords:
primary hyperoxaluria;
rna interference;
known types;
ldha inhibition ... See more keywords