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Production and characterization of erythropoietic protoporphyric heterodimeric ferrochelatases

Mutations resulting in diminished activity of the dimeric enzyme ferrochelatase are a prerequisite for the inherited disorder erythropoietic protoporphyria (EPP). Patients with clinical EPP have only 10% to 30% of normal levels of ferrochelatase activity, and although many patients with EPP have one...

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Detalhes bibliográficos
Main Authors: Najahi-Missaoui, Wided, Dailey, Harry A.
Formato: Artigo
Idioma:Inglês
Publicado em: © 2005 by The American Society of Hematology 2005
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1473221/
https://ncbi.nlm.nih.gov/pubmed/15831704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2004-12-4661
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