Litiasis due to 2,8-dihydroxyadenine, usefulness of the genetic study
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference17 articles.
1. Genetic defects underlying renal stone disease;Rumsby;Int J Surg,2016
2. 2,8-Dihydroxyadenine urolithiasis: a not so rare inborn error of purine metabolism;Ceballos-Picot;Nucleosides Nucleotides Nucleic Acids,2014
3. Quiz page May 2015: crystalline nephropathy in an identical twin;Agrawal;Am J Kidney Dis,2015
4. Kidney disease in adenine phosphoribosyltransferase deficiency;Runolfsdottir;Am J Kidney Dis,2016
5. Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man;Kelley;J Clin Investig,1968
Cited by 1 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
1. Recurrence of 2,8-dihydroxyadenine Crystalline Nephropathy in a Kidney Transplant Recipient: A Case Report and Literature Review;Internal Medicine;2021-08-15
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