| pubmed-article:16280445 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C0027567 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C0302583 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C0449438 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C0915115 | lld:lifeskim |
| pubmed-article:16280445 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:16280445 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:16280445 | pubmed:dateCreated | 2005-11-10 | lld:pubmed |
| pubmed-article:16280445 | pubmed:abstractText | Iron deficiency is common in African children, but genetic variations affecting susceptibility have not been identified. The Q248H mutation in ferroportin, a cellular iron exporter regulated by iron status and inflammation, may be associated with high iron stores in African adults. | lld:pubmed |
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| pubmed-article:16280445 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16280445 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:16280445 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16280445 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:16280445 | pubmed:issn | 0002-9165 | lld:pubmed |
| pubmed-article:16280445 | pubmed:author | pubmed-author:KasvosveIshma... | lld:pubmed |
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| pubmed-article:16280445 | pubmed:author | pubmed-author:MatibePetrone... | lld:pubmed |
| pubmed-article:16280445 | pubmed:author | pubmed-author:MudengeBonifa... | lld:pubmed |
| pubmed-article:16280445 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16280445 | pubmed:volume | 82 | lld:pubmed |
| pubmed-article:16280445 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16280445 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16280445 | pubmed:pagination | 1102-6 | lld:pubmed |
| pubmed-article:16280445 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:16280445 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16280445 | pubmed:articleTitle | Effect of ferroportin Q248H polymorphism on iron status in African children. | lld:pubmed |
| pubmed-article:16280445 | pubmed:affiliation | Department of Chemical Pathology, University of Zimbabwe College of Health Sciences, Harare, Zimbabwe. ikasvosve@medsch.uz.ac.zw | lld:pubmed |
| pubmed-article:16280445 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16280445 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:16280445 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:16280445 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16280445 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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