|
1
|
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.
|
Nat Genet
|
2003
|
5.82
|
|
2
|
Hepcidin in iron overload disorders.
|
Blood
|
2005
|
2.88
|
|
3
|
The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.
|
Haematologica
|
2006
|
2.80
|
|
4
|
The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
|
Haematologica
|
2004
|
0.86
|
|
5
|
Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece.
|
Haematologica
|
2004
|
0.78
|
|
6
|
Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE.
|
Blood Cells Mol Dis
|
2006
|
0.76
|
|
7
|
Arthropathy in juvenile hemochromatosis.
|
Arthritis Rheum
|
2003
|
0.75
|