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Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data
BACKGROUND: Hereditary hemochromatosis (HH) is a common inherited disorder of iron metabolism in Northern European populations. The discovery of a candidate gene in 1996 (HFE), and of its main mutation (C282Y), has radically altered the way to diagnose this disease. The aim of this study was to asse...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2005
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1180708/ https://ncbi.nlm.nih.gov/pubmed/15929798 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-6-24 |
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