Corrigendum to: Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV [Blood Cells Mol. Dis. 40:3 (2008) 353–359]
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Published in | Blood cells, molecules, & diseases Vol. 51; no. 1; p. 69 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.06.2013
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Online Access | Get full text |
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