Phenotype and HFE genotype in a population with abnormal iron markers recruited from an Endocrinology Department
Author(s) -
MarieChristine Vantyghem,
Isabelle Fajardy,
Florence Dhondt,
Caroline Girardot,
Michèle d’Herbomez,
Pierre-Marie Danzé,
Jean Rousseaux,
Jean-Louis Wémeau
Publication year - 2006
Publication title -
european journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 148
eISSN - 1479-683X
pISSN - 0804-4643
DOI - 10.1530/eje.1.02152
Subject(s) - medicine , genotype , endocrinology , allele frequency , population , allele , genotyping , transferrin saturation , ferritin , loss of heterozygosity , biology , hereditary hemochromatosis , body mass index , genotype frequency , genetics , hemochromatosis , serum ferritin , gene , environmental health
The aim of this study was to describe HFE genotype in a population of patients with altered iron markers recruited in an Endocrinology Department and to define the possible phenotype-genotype relationships.
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