Andere Kunden interessierten sich auch für
![Interferon beta 1 gene and human cancer]( "Interferon beta 1 gene and human cancer")
Interferon beta 1 gene and human cancer32,99 €![Genetic mutations in beta-thalassemia disease]( "Genetic mutations in beta-thalassemia disease")
Genetic mutations in beta-thalassemia disease39,99 €![Function of beta cell and extracellular RNAs as potential biomarker]( "Function of beta cell and extracellular RNAs as potential biomarker")
Function of beta cell and extracellular RNAs as potential biomarker51,99 €![Multiplex High-Resolution Melting Analysis as a Diagnostic Tool]( "Multiplex High-Resolution Melting Analysis as a Diagnostic Tool")
Multiplex High-Resolution Melting Analysis as a Diagnostic Tool52,99 €![Beta Thalassemia Mutations in Sudanese Patients]( "Beta Thalassemia Mutations in Sudanese Patients")
Beta Thalassemia Mutations in Sudanese Patients26,99 €![The Molecular Clock of Human Embryonic Heart]( "The Molecular Clock of Human Embryonic Heart")
The Molecular Clock of Human Embryonic Heart39,99 €![Human Lectins in Parasitic Infections: Friend or Foe?]( "Human Lectins in Parasitic Infections: Friend or Foe?")
Human Lectins in Parasitic Infections: Friend or Foe?38,99 €
Thalassemia is an important hematological disorder. The possibility of iron overload development may be increase by Interaction between thalassemia and HFE gene mutations. This study aim to investigate the possible association between serum hepcidin level as indicator of iron concentration and the presence of HFE gene mutations. Excess iron overload increases the risk of liver cirrhosis,cancer,hypogonadism,arthritis, cardiac arrhythmia, heart failure, retinal degeneration, diabetes mellitus, neurodegenerative diseases (Alzheimer's,Parkinson's, Huntington's), and premature death.