Primary hyperoxaluria type 1: Genotypic and phenotypic heterogeneity
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF00711363
Reference29 articles.
1. Allsop J, Jennings PR, Danpure CJ (1987) A new micro-assay for human liver alanine: glyoxylate aminotransferase.Clin Chim Acta 170: 187?193.
2. Cooper PJ, Danpure CJ, Wise PJ, Guttridge KM (1988) Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.J Histochem Cytochem 36: 1285?1294.
3. Danpure CJ (1989) Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.J Inher Metab Dis 12: 210?224.
4. Danpure CJ (1991) Molecular and clinical heterogeneity in primary hyperoxaluria type 1.Am J Kidney Dis 17: 366?369.
5. Danpure CJ, Jennings PR (1986) Peroxisomal alanine: glyoxylate aminotransferase deficiency in primary hyperoxaluria type I.FEBS Lett 201: 20?24.
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