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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Scotet, Virginie, Le Gac, Gérald, Mérour, Marie-Christine, Mercier, Anne-Yvonne, Chanu, Brigitte, Ka, Chandran, Mura, Catherine, Nousbaum, Jean-Baptiste, Férec, Claude
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2005
Materias:
Research Article
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares