Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient
Blood
Gut
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2q32 Google OMIM PubMed [Hemochromatosis] Hemochromatosis, type 4 *Gene map locus 2q32 HFE4 Hemochromatosis due to defect in ferroportin Hemochromatosis, autosomal dominant [Clinical features: iron overload resulting in hepatic fibrosis, diabetes, impotence, and arrhythmias] [Inheritance: autosomal dominant] |
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Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis |
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient |
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Blood |
Gut |
