A stone in the bone

Primary hyperoxaluria (PH) is a group of diseases due to mutations in genes coding for enzymes involved in oxalate metabolism. Three types of PH are identified depending on the gene mutated. Type 1 is the most frequent with 80% of the cases, while PH2 and PH3 are rarer. The severity of renal involve...

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Detalles Bibliográficos
Autores principales: Halfon, Matthieu, Cochat, Pierre, Kissling, Sebastien, Dattner, Nicolas, de Leval, Laurence, Fakhouri, Fadi, Pruijm, Menno, Bonny, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Images in Metabolic Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574174/
https://www.ncbi.nlm.nih.gov/pubmed/34765391
http://dx.doi.org/10.1002/jmd2.12246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574174/
https://www.ncbi.nlm.nih.gov/pubmed/34765391
http://dx.doi.org/10.1002/jmd2.12246

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