Author:
Leumann Ernst,Hoppe Bernd
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Reference18 articles.
1. Danpure CJ (2004) Molecular aetiology of primary hyperoxaluria type 1. Nephron Exp Nephrol 98:E39?44
2. Hoppe B, Langman CB (2003) A United States survey on diagnosis, treatment, and outcome of primary hyperoxaluria. Pediatr Nephrol 18:986?991
3. van Woerden CS, Groothoff JW, Wijburg FA, Annink C, Wanders RJ, Waterham HR (2004) Clinical implications of mutation analysis in primary hyperoxaluria type 1. Kidney Int 66:746?752
4. von Schnakenburg C, Latta K (2002) Hyperoxaluria. In: Blau N, Duran M, Blaskovics ME, Gibson KM (eds) Physician?s guide to the laboratory diagnosis of metabolic diseases, 2nd edn. Springer, Berlin Heidelberg New York, pp 505?518
5. Zhang X, Roe SM, Hou Y, Bartlam M, Rao Z, Pearl LH, Danpure CJ (2003) Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1. J Mol Biol 331:643?652
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