Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Reference23 articles.
1. Danpure CJ. Primary hyperoxaluria. In: Scriver CR, Beaudet AL, Sly WS et al. eds. The Metabolic and Molecular Bases of Inherited Disease. McGraw-Hill, New York: 2001; 3323–3367
2. Danpure CJ, Rumsby G. Molecular aetiology of primary hyperoxaluria and its implications for clinical management. Expert Rev Mol Med2004; 6: 1–16
3. Takada Y, Kaneko N, Esumi H, Purdue PE, Danpure CJ. Human peroxisomal l-alanine:glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon. Biochem J1990; 268: 517–520
4. Purdue PE, Lumb MJ, Fox M et al. Characterization and chromosomal mapping of a genomic clone encoding human alanine: glyoxylate aminotransferase. Genomics1991; 10: 34–42
5. Rumsby G, Cregeen DP. Identification and expression of a cDNA for human hydroxypyruvate/glyoxylate reductase. Biochim Biophys Acta1999; 1446: 383–388
Cited by
34 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献