1. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type 1,1986
2. Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase;Purdue, P.E.; Lumb, M.J.; Fox, M.;Genomics,1991
3. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity;Danpure, C.J.; Jennings, P.R.; Fryer, P.; Purdue, P.E.; Allsop, J.;J Inherit Metab Dis,1994
4. Primary hyperoxaluria type;Latta, K.; Brodehl, J.;I. EurJ7 Pediatr,1990
5. Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation;Watts, R.W.; Calne, R.Y.; Rolles, K.;Lancet,1987