Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type

Author:

Mandrile Giorgia,van Woerden Christiaan S.,Berchialla Paola,Beck Bodo B.,Acquaviva Bourdain Cécile,Hulton Sally-Anne,Rumsby Gill

Publisher

Elsevier BV

Subject

Nephrology

Reference28 articles.

1. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I;Danpure;FEBS Lett,1986

2. Calcium oxalate crystals induce renal inflammation by NLRP3-mediated IL-1beta secretion;Mulay;J Clin Invest,2013

3. Primary hyperoxaluria type 1: strategy for organ transplantation;Cochat;Curr Opin Organ Transplant,2010

4. Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene;Williams;Hum Mutat,2009

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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