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Primary hyperoxaluria type 1 in developing countries: novel challenges in a new therapeutic era
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive inborn error of metabolism characterized by marked hepatic overproduction of oxalate due to deficiency of hepatic peroxisomal alanine-glyoxylate aminotransferase caused by AGXT gene mutation. One major hallmark of PH1 in developed as well...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113489/ https://www.ncbi.nlm.nih.gov/pubmed/35592622 http://dx.doi.org/10.1093/ckj/sfab203 |