|
Volumn 12, Issue 6, 2000, Pages 596-602
|
Inherited iron overload disorders
|
Author keywords
[No Author keywords available]
|
Indexed keywords
IRON;
CLINICAL FEATURE;
DISEASE COURSE;
GENE MUTATION;
GENETIC ASSOCIATION;
HEMOCHROMATOSIS;
HUMAN;
IRON METABOLISM;
IRON OVERLOAD;
PATHOGENESIS;
PRIORITY JOURNAL;
REVIEW;
SMALL INTESTINE ABSORPTION;
HEMOCHROMATOSIS;
HUMANS;
|
EID: 0033730996
PISSN: 10408703
EISSN: None
Source Type: Journal
DOI: 10.1097/00008480-200012000-00015 Document Type: Review |
Times cited : (12)
|
References (68)
|