Parcourir par auteur "Christakis, J."
Voici les éléments 1-3 de 3
-
Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
Speletas, M.; Kioumi, A.; LouleS, G.; Hytiroglou, P.; Tsitouridis, J.; Christakis, J.; GermeniS, A. E. (2008)Mutations in the SLC40Al gene result in a dominant genetic disorder [ferroportin disease; hereditary hemochromatosis type (HH) IV], characterized by iron overload with two different clinical manifestations, normal transferrin ... -
Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV (vol 40, pg 353, 2008)
Speletas, M.; Kioumi, A.; Loules, G.; Hytiroglou, P.; Tsitouridis, J.; Christakis, J.; Germenis, A. E. (2013) -
Analysis of SLC40A1(Ferroportin 1) gene at mrna level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV
Speletas, M.; Kioumi, A.; Loules, G.; Kalala, F.; Katodritou, E.; Tsitouridis, I.; Hytiroglou, P.; Christakis, J.; Korantzis, I.; Germenis, A. (2007)