Chromosomal localization, hematologic characterization, and iron metabolism of the hereditary erythroblastic anemia (hea) mutant mouse
Author:
Affiliation:
1. From Medical Research, Children's Mercy Hospitals and Clinics, University of Missouri Kansas City, Kansas City, MO; University of Kansas Medical Center, Kansas City, KS; and Naruto University of Education, Naruto, Japan.
Abstract
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/104/5/1511/1701045/zh801704001511.pdf
Reference31 articles.
1. Feder JN, Gnirke A, Thomas W, et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996;13: 399-408.
2. Fleming MD, Trenor CC, Su MA, et al. Microcytic anemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nat Genet. 1997;16: 383-386.
3. Vulpe CD, Kuo YM, Murphy TL, et al. Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse. Nat Genet. 1999;21: 195-199.
4. Donovan A, Brownlie A, Zhou Y, et al. Positional cloning of zebrafish ferroportin-1 identifies a conserved vertebrate iron exporter. Nature. 2000;403: 776-781.
5. Edwards JA, Hoke JE. Red cell iron uptake in hereditary microcytic anemia. Blood. 1975;46: 381-388.
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