Title : Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis.

Pub. Date : 2004 Sep-Oct

PMID : 15464418






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 The disease is caused by a deficiency of alanine:glyoxylate aminotransferase (AGT) which catalyzes the conversion of glyoxylate to glycine. Glycine alanine--glyoxylate and serine--pyruvate aminotransferase Homo sapiens
2 The disease is caused by a deficiency of alanine:glyoxylate aminotransferase (AGT) which catalyzes the conversion of glyoxylate to glycine. Glycine alanine--glyoxylate and serine--pyruvate aminotransferase Homo sapiens