Therapeutic strategies for acute intermittent porphyria

Acute intermittent porphyria (AIP) is an autosomal dominant disease caused by mutations in porphobilinogen deaminase (PBGD), the third enzyme of the heme synthesis pathway. Symptoms of AIP usually manifest as intermittent acute attacks with occasional neuropsychiatric crises. The management of AIP i...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Intractable Rare Dis Res
Main Authors: Zhao, Lanlan, Wang, Xinyang, Zhang, Xiaoning, Liu, Xiantao, Ma, Ningzhen, Zhang, Yiran, Zhang, Songyun
Format: Artigo
Jezik:Inglês
Izdano: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2020
Teme:
Review
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7586882/
https://ncbi.nlm.nih.gov/pubmed/33139979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2020.03089
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