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Acute intermittent porphyria: focus on possible mechanisms of acute and chronic manifestations
Porphyrias are a group of inherited metabolic diseases that include eight types, each of which is caused by a mutation that affects an enzyme of the heme biosynthetic pathway. When an enzyme defect has physiological significance, it leads to overproduction of pathway precursors prior to the defectiv...
Uloženo v:
| Vydáno v: | Intractable Rare Dis Res |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7586881/ https://ncbi.nlm.nih.gov/pubmed/33139977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2020.03054 |
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