Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference26 articles.
1. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I;Danpure;FEBS Lett,1986
2. Primary hyperoxaluria;Danpure,2001
3. Epidemiology of primary hyperoxaluria type 1. Societe de Nephrologie and the Societe de Nephrologie Pediatrique;Cochat;Nephrol Dial Transplant,1995
4. Primary hyperoxaluria type I;Latta;Eur J Pediatr,1990
5. AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria;Amoroso;J Am Soc Nephrol,2001
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