A molecular defect in human protoporphyria.

Protoporphyria is generally an autosomal dominant disease that is characterized clinically by photosensitivity and hepatobiliary disease and that is characterized biochemically by elevated protoporphyrin levels. The enzymatic activity of ferrochelatase, which catalyzes the last step in the heme bios...

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Bibliografski detalji
Glavni autori: Brenner, D A, Didier, J M, Frasier, F, Christensen, S R, Evans, G A, Dailey, H A
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682545/
https://ncbi.nlm.nih.gov/pubmed/1376018
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