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Article

A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overload

5 Apr 2006

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Share to Hemoglobinopathies and Related Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16584902
DOI: 10.1016/j.bcmd.2006.01.011

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Related research

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A novel R416C mutation in human DMT1 (SLC11A2) displays pleiotropic effects on function and causes microcytic anemia and hepatic iron overloadPMID 16584902Read ↗

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A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload.Semantic proximity Read ↗

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The Spectra of Disease-Causing Mutations in the Ferroportin 1 (SLC40A1) Encoding Gene and Related Iron Overload Phenotypes (Hemochromatosis Type 4 and Ferroportin Disease)Semantic proximity Read ↗

Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.Semantic proximity Read ↗

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