| Literature DB >> 9241278 |
M D Fleming1, C C Trenor, M A Su, D Foernzler, D R Beier, W F Dietrich, N C Andrews.
Abstract
Although disorders of iron metabolism are prevalent, iron transport remains poorly understood. To address this problem, we undertook a positional cloning strategy to identify the causative mutation in mice with microcytic anaemia (mk). Homozygous mk/mk mice have microcytic, hypochromic anaemia due to severe defects in intestinal iron absorption and erythroid iron utilization. We report the identification of a strong candidate gene for mk, and suggest that the phenotype is a consequence of a missense mutation in Nramp2 (ref. 5), a previously identified gene of unknown function. Nramp2 is homologous to Nramp1, a gene activa in host defense. If Nramp2 is mk, as the cumulative evidence suggests, our findings have broad implications for the understanding of iron transport and resistance to intracellular pathogens.Entities:
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Year: 1997 PMID: 9241278 DOI: 10.1038/ng0897-383
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330