Hemochromatosis C282Y gene mutation as a potential susceptibility factor for iron-overload in Egyptian beta-thalassemia patients
Egyptian Journal of Medical Human Genetics [The]. 2018; 19 (2): 103-106
Dans Anglais
| IMEMR
| ID: emr-192878
ABSTRACT
Background:
Hereditary hemochromatosis is the most frequent cause of primary iron overload that is associated with HFE gene's mutation especially the C282Y mutation. The interaction between hemoglobin chain synthesis' disorders and the C282Y mutation may worsen the clinical picture of betathalassemia major [b-TM]
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Indice:
Méditerranée orientale
langue:
Anglais
Texte intégral:
Egypt. J. Med. Hum. Genet.
Année:
2018
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