Title : [Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].

Pub. Date : 2019 Dec 31

PMID : 32003182






1 Functional Relationships(s)
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1 The mutations in the AGXT, GRHPR, HOGA1 genes are attributable for different types of primary hyperoxaluria leading to the dysfunction of specific enzymes involved in the oxalate metabolism. Oxalates alanine--glyoxylate and serine--pyruvate aminotransferase Homo sapiens