Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

BACKGROUND: Hereditary hemochromatosis (HH) is a common autosomal recessive disorder in populations of European descent. It is characterized by a variable prevalence of mutations in the hemochromatosis gene (HFE) in different countries and a complex relationship between the HFE genotype and the HH p...

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Detalhes bibliográficos
Main Authors: Milić, Sandra, Ristić, Smiljana, Starčević-Čizmarević, Nada, Brajenović-Milić, Bojana, Crnić-Martinović, Marija, Kapović, Miljenko, Peterlin, Borut, Štimac, Davor
Formato: Artigo
Idioma:Inglês
Publicado em: International Scientific Literature, Inc. 2011
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3539475/
https://ncbi.nlm.nih.gov/pubmed/21959608
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/MSM.881980
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