@article{detivaud:hal-00876616,
TITLE = {Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.},
AUTHOR = {D{\'e}tivaud, L{\'e}na{\"i}ck and Island, Marie-Laure and Jouanolle, Anne-Marie and Ropert, Martine and Bardou-Jacquet, Edouard and Le Lan, Caroline and Mosser, Annick and Leroyer, Patricia and Deugnier, Yves and David, V{\'e}ronique and Brissot, Pierre and Lor{\'e}al, Olivier},
URL = {https://hal.science/hal-00876616},
JOURNAL = {Human Mutation},
PUBLISHER = {Wiley},
VOLUME = {34},
NUMBER = {11},
PAGES = {1529-36},
YEAR = {2013},
MONTH = Nov, DOI = {10.1002/humu.22396},
KEYWORDS = {ferroportin ; iron overload ; hemochromatosis ; hepcidin ; SLC40A1},
HAL_ID = {hal-00876616},
HAL_VERSION = {v1},
}