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Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation.

Protoporphyria is a genetic disorder in which a deficiency of mitochondrial ferrochelatase activity causes accumulation of protoporphyrin that produces severe liver damage in some patients. In this study, mutations of the ferrochelatase gene were examined in eight unrelated patients who had liver tr...

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Podrobná bibliografie
Vydáno v:J Clin Invest
Hlavní autoři: Bloomer, J, Bruzzone, C, Zhu, L, Scarlett, Y, Magness, S, Brenner, D
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Clinical Investigation 1998
Témata:
On-line přístup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC509071/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9649563/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI1347
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