PEROXISOMAL ALANINE:GLYOXYLATE AMINOTRANSFERASE AND PRENATAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1
- 15 November 1986
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 328 (8516) , 1168
- https://doi.org/10.1016/s0140-6736(86)90584-2
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986
- FETAL LIVER BIOPSY FOR PRENATAL DIAGNOSIS OF ORNITHINE CARBAMYL TRANSFERASE DEFICIENCYThe Lancet, 1982
- The organ distribution of human alanine-2-oxoglutarate aminotransferase and alanine-glyoxylate aminotransferaseBiochemical Medicine, 1980