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Normal reference ranges for urinary δ‐aminolevulinic acid and porphobilinogen levels

Acute hepatic porphyria (AHP) is a family of rare, serious, and potentially life‐threatening metabolic disorders caused by mutations in genes encoding enzymes involved in hepatic heme biosynthesis. AHP is characterized by accumulation of neurotoxic heme intermediates, δ‐aminolevulinic acid (ALA), an...

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Detalles Bibliográficos
Autores principales:	Agarwal, Sagar, Habtemarium, Bahru, Xu, Yuanxin, Simon, Amy R., Kim, Jae B., Robbie, Gabriel J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons, Inc. 2020
Materias:	Research Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802627/ https://www.ncbi.nlm.nih.gov/pubmed/33473344 http://dx.doi.org/10.1002/jmd2.12173

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