Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria

Congenital erythropoietic porphyria, an autosomal recessive inborn error of heme biosynthesis, results from the markedly deficient activity of uroporphyrinogen III synthase. Extensive mutation analyses of 40 unrelated patients only identified approximately 90% of mutant alleles. Sequencing the recen...

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Detalles Bibliográficos

Publicado en:	J Clin Invest
Principais autores:	Solis, Constanza, Aizencang, Gerardo I., Astrin, Kenneth H., Bishop, David F., Desnick, Robert J.
Formato:	Artigo
Idioma:	Inglês
Publicado:	American Society for Clinical Investigation 2001
Assuntos:	Article
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC208941/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11254675/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI10642
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