Identification of a ferrochelatase mutation in a Chinese family with erythropoietic protoporphyria
Author:
Publisher
Elsevier BV
Subject
Hepatology
Reference22 articles.
1. Erythropoietic protoporphyria;Todd;Br J Dermatol,1994
2. Molecular defects in ferrochelatase in patients with protoporphyria requiring liver transplantation;Bloomer;J Clin Invest,1998
3. Liver transplantation for erythropoietic protoporphyria liver disease;McGuire;Liver Transpl,2005
4. Structure of the human ferrochelatase gene. Exon/intron gene organization and location of the gene to chromosome 18;Taketani;Eur J Biochem,1992
5. Ferrochelatase activity in human lymphocytes, as quantified by a new high-performance liquid-chromatographic method;Rossi;Clin Chem,1988
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