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Primary hyperoxaluria type 1: time for prime time?

Oxalate crystals in the kidney were first described in 1925. Since then, many major milestones have been reached in the understanding of genetic primary hyperoxaluria(s). Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disease due to a mutation in the AGXT gene, which encodes the hepati...

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Detalles Bibliográficos
Autores principales: Bacchetta, Justine, Wood, Kyle D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113466/
https://www.ncbi.nlm.nih.gov/pubmed/35592621
http://dx.doi.org/10.1093/ckj/sfab233

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