@article{brissot:hal-01671715,
TITLE = {Genetic hemochromatosis: Pathophysiology, diagnostic and therapeutic management},
AUTHOR = {Brissot, P. and Cavey, T. and Ropert, M. and Guggenbuhl, P. and Lor{\'e}al, Olivier},
URL = {https://univ-rennes.hal.science/hal-01671715},
JOURNAL = {La Presse M{\'e}dicale},
PUBLISHER = {Elsevier Masson},
VOLUME = {46},
NUMBER = {12},
PAGES = {e288-e295},
YEAR = {2017},
MONTH = Dec, DOI = {10.1016/j.lpm.2017.05.037},
KEYWORDS = {TFR2 gene ; symptomatology ; supplementation ; SLC40A1 gene ; Short Survey ; sex difference ; phlebotomy ; pathophysiology ; iron overload ; iron chelation ; hyperferritinemia ; HFE2 gene ; human ; ferroportin ; hepcidin ; apheresis ; cell transport ; chromosome 1 ; chromosome 19 ; chromosome 2 ; chromosome 3 ; chromosome 7 ; disease classification ; erythocytapheresis ; gene ; genetic screening ; HAMP gene ; hemochromatosis ; HFE gene},
PDF = {https://univ-rennes.hal.science/hal-01671715/file/Brissot%20-%20Genetic%20hemochromatosis.pdf},
HAL_ID = {hal-01671715},
HAL_VERSION = {v1},
}