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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Scotet, Virginie, Le Gac, Gérald, Mérour, Marie-Christine, Mercier, Anne-Yvonne, Chanu, Brigitte, Ka, Chandran, Mura, Catherine, Nousbaum, Jean-Baptiste, Férec, Claude
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2005
Gaiak:
Research Article
Sarrera elektronikoa: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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