| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8469509 | Egyptian Journal of Medical Human Genetics | 2018 | 4 Pages |
Abstract
The C282Y mutation was not detected in the studied cohort of Egyptian β-TM patients neither in homozygous nor heterozygous state in spite of manifestations of iron overload complications.
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Authors
G.M. Mokhtar, M.S. El Alfy, F.S.E. Ebeid, M.A. El Sawi, M.H. Fayek, A.A.M. Adly, Asama Zaki,