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Polymorphisms of hemochromatosis, and alpha-1 antitrypsin genes in Egyptian HCV patients with and without hepatocellular carcinoma
Faculty
Medicine
Year:
2011
Type of Publication:
ZU Hosted
Pages:
Authors:
Rehab Ahmed Karam Abdelfattah
Staff Zu Site
Abstract In Staff Site
Journal:
gene elsiever
Volume:
Keywords :
Polymorphisms , hemochromatosis, , alpha-1 antitrypsin genes , Egyptian
Abstract:
Hereditary hemochromatosis and alpha-1antitrypsin deficiency are genetic diseases characterized by endoplasmic reticulum (ER) stress with subsequent development of liver disease. Our aim was to estimate the frequency of hemochromatosis gene
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Osama Abdelaziz Mahmoud Mahmoud, "Factor VIII inhibitor development in Egyptian hemophilia patients: does intron 22 inversion mutation play a role?", italian j of pediatric, 2020
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Rania Ahmed Foad, "Association of Plasminogen Activator Inhibitor 1 (PAI-1) 4G/5G Polymorphism and Susceptibility to SLE in Egyptian Children and Adolescents: A Multicenter Study", Dove press, 2020
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