Iron load
Recent research addressed the main role of hepcidin in the regulation of iron metabolism. However, while this mechanism could be relevant in causing iron load in Thalassemia Intermedia and Sickle-Cell Anemia, its role in Thalassemia Major (TM) is marginal. This is mainly due to the high impact of tr...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2013-03-01
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Series: | Thalassemia Reports |
Online Access: | http://www.pagepressjournals.org/index.php/thal/article/view/1473 |