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Primary Hyperoxaluria

The primary hyperoxalurias are a group of autosomal recessive disorders of endogenous oxalate overproduction. This review discusses the major biochemical, genetic, and therapeutic advances that have led to a better understanding of the disease.

Journal Title: The New England Journal of Medicine Aug 15, 2013, Vol.369(7), pp.649-658
Main Author: Cochat Pierre
Format: Electronic Article Electronic Article
Language: English
Subjects:
ID: ISSN: 00284793 ; E-ISSN: 15334406 ; DOI: 10.1056/NEJMra1301564
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title: Primary Hyperoxaluria
format: Article
creator:
  • Cochat Pierre
subjects:
  • Spain
  • Europe
  • Diet
  • Primary Hyperoxaluria
  • Enzymes
  • Dehydrogenases
  • Hyperoxaluria
  • Kidney Diseases
  • Oxalic Acid
ispartof: The New England Journal of Medicine, Aug 15, 2013, Vol.369(7), pp.649-658
description: The primary hyperoxalurias are a group of autosomal recessive disorders of endogenous oxalate overproduction. This review discusses the major biochemical, genetic, and therapeutic advances that have led to a better understanding of the disease.
language: eng
source:
identifier: ISSN: 00284793 ; E-ISSN: 15334406 ; DOI: 10.1056/NEJMra1301564
fulltext: fulltext
issn:
  • 00284793
  • 0028-4793
  • 15334406
  • 1533-4406
url: Link


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abstractThe primary hyperoxalurias are a group of autosomal recessive disorders of endogenous oxalate overproduction. This review discusses the major biochemical, genetic, and therapeutic advances that have led to a better understanding of the disease.
copBoston
pubMassachusetts Medical Society
doi10.1056/NEJMra1301564
urlhttp://search.proquest.com/docview/1424396923/
date2013-08-15