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Cite This Article
BEYAN, C., BEYAN, E. (2018). A rare cause of hereditary hemochromatosis: homozygous H63D. Cukurova Medical Journal, Cilt: 43 - Sayı: Ek 1, 330–332. https://ajindex.com/articles/119843
Journals / Cukurova Medical Journal / 2018 / Cilt: 43 - Sayı: Ek 1
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