Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency)

J Inherit Metab Dis. 1988:11 Suppl 2:205-7. doi: 10.1007/BF01804236.

Authors

C J Danpure¹, P R Jennings

Affiliation

¹ Division of Inherited Metabolic Diseases, Clinical Research Centre, Harrow, UK.

PMID: 3141703
DOI: 10.1007/BF01804236

No abstract available

MeSH terms

Alanine Transaminase / deficiency*
Humans
Hyperoxaluria / enzymology*
Liver / enzymology*
Microbodies / enzymology*
Oxalates / urine
Oxalic Acid
Transaminases*

Substances

Oxalates
Oxalic Acid
Transaminases
Alanine Transaminase
Alanine-glyoxylate transaminase