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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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| Publicado no: | Hepatol Commun |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | 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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