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authFullName_s : C. Le Lan

Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis

H. Hamdi-Rozé , M.-P. Beaumont-Epinette , Z. Ben Ali , C. Le Lan , V. Loustaud-Ratti et al.
American Journal of Hematology, 2016, 91 (12), pp.1202--1205. ⟨10.1002/ajh.24535⟩
Journal articles hal-01427007v1