Title : Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2.

Pub. Date : 2003 Dec

PMID : 14635115






1 Functional Relationships(s)
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1 Primary hyperoxaluria type 2, an inherited autosomal recessive disorder of endogenous oxalate overproduction, is caused by mutations in the GRHPR gene encoding the glyoxylate/hydroxypyruvate reductase enzyme. Oxalates glyoxylate and hydroxypyruvate reductase Homo sapiens