海西定
血色病
遗传性血色病
突变
汉普
基因
遗传学
铁转运蛋白
内科学
生物
医学
内分泌学
贫血
作者
Daniel F. Wallace,Jeannette L. Dixon,Grant A. Ramm,Gregory J. Anderson,Lawrie W. Powell,V. Nathan Subramaniam
出处
期刊:PubMed
[National Institutes of Health]
日期:2005-02-01
卷期号:90 (2): 254-5
被引量:22
摘要
Juvenile hemochromatosis is a severe form of hereditary iron overload. It can be caused by mutations in either hepcidin or hemojuvelin genes. In this study we identified the molecular basis of juvenile hemochromatosis in three Australian families and assessed the role of potential modifying genes in individuals carrying HFE mutations.
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