Pub. Date : 2003 Dec
PMID : 14635115
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
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 |