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A Japanese Family with Ferroportin Disease Caused by a Novel Mutation of SLC40A1 Gene: Hyperferritinemia Associated with a Relatively Low Transferrin Saturation of Iron
KOYAMA, Chizu, WAKUSAWA, Shinya, HAYASHI, Hisao, UENO, Toshio, SUZUKI, Rie, YANO, Motoyoshi, SAITO, Hiroshi, OKAZAKI, ToruVolume:
44
Year:
2005
Language:
english
Journal:
Internal Medicine
DOI:
10.2169/internalmedicine.44.990
File:
PDF, 147 KB
english, 2005