Primary Hyperoxaluria
- Author
- COCHAT, Pierre1 ; RUMSBY, Gill2
[1] Centre de Référence des Maladies Rénales Rares Néphrogones; Centre de la Recherche Scientifique — Unité Mixte de la Recherche 5305, Hospices Civils de Lyon, and Université Claude-Bernard Lyon 1, Lyon, France
[2] Clinical Biochemistry, University College London Hospitals, London, United Kingdom - Source
The New England journal of medicine. 2013, Vol 369, Num 7, pp 649-658, 10 p ; ref : 72 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Waltham, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Hyperoxalurie Médecine Oxalate Primaire Enzymopathie Maladie héréditaire Maladie métabolique
- Keyword (en)
- Hyperoxaluria Medicine Oxalate Primary Enzymopathy Genetic disease Metabolic diseases
- Keyword (es)
- Hiperoxaluria Medicina Oxalato Primario Enzimopatía Enfermedad hereditaria Metabolismo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D05 Miscellaneous hereditary metabolic disorders
- Discipline
- Generalities in medical sciences Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 27583607
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1056/NEJMra1301564 
https://dx.doi.org/10.1056/NEJMra1301564
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