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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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| Vydáno v: | Hepatol Commun |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2018
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| Témata: | |
| On-line přístup: | 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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