Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease.

A viable autosomal recessive mutation (named fch, or ferrochelatase deficiency) causing jaundice and anemia in mice arose in a mutagenesis experiment using ethylnitrosourea. Homozygotes (fch/fch) display a hemolytic anemia, photosensitivity, cholestasis, and severe hepatic dysfunction. Protoporphyri...

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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Tutois, S, Montagutelli, X, Da Silva, V, Jouault, H, Rouyer-Fessard, P, Leroy-Viard, K, Guénet, J L, Nordmann, Y, Beuzard, Y, Deybach, J C
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1991
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295715/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1939658/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115491
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