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Acute Hepatic Porphyrias: Review and Recent Progress
The acute hepatic porphyrias (AHPs) are a group of four inherited diseases of heme biosynthesis that present with episodic, acute neurovisceral symptoms. The four types are 5‐aminolevulinic acid (ALA) dehydratase deficiency porphyria, acute intermittent porphyria, hereditary coproporphyria, and vari...
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| Publié dans: | Hepatol Commun |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
John Wiley and Sons Inc.
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6357830/ https://ncbi.nlm.nih.gov/pubmed/30766957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep4.1297 |
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