Coexistence of β-Thalassemia and Hereditary Hemochromatosis in Homozygosity: A Possible Synergic Effect?

A few considerations, which we found in the literature, inspired us to reevaluate patients previously investigated [characterized for β-thalassemia (β-thal) and hereditary hemochromatosis (HH) genes] by our department at Medical Genetics, School of Medicine, University of Foggia, Italy.

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Veröffentlicht in:Hemoglobin 2009, Vol.33 (2), p.155-157, Article 155
Hauptverfasser: Bukvic, Nenad, Sportelli, Filomena, Sessa, Francesco, Longo, Vittoria, Roberti, Maria Grazia, Santacroce, Rosa, Margaglione, Maurizio
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Sprache:eng
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Zusammenfassung:A few considerations, which we found in the literature, inspired us to reevaluate patients previously investigated [characterized for β-thalassemia (β-thal) and hereditary hemochromatosis (HH) genes] by our department at Medical Genetics, School of Medicine, University of Foggia, Italy.
ISSN:0363-0269
1532-432X
DOI:10.1080/03630260902817354