Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis

Keyphrases

• Alignment Programs 20%
• Chinese Case 20%
• Chinese Patients 100%
• Chinese Population 40%
• Clinical Features 20%
• Ferroportin 40%
• Gene Sequencing 20%
• Hemochromatosis 20%
• Hemojuvelin 20%
• Hepcidin 20%
• Hereditary Hemochromatosis 100%
• HFE2 100%
• Intolerant 20%
• Iron Overload Disorders 20%
• Missense mutation 20%
• Molecular Consequences 20%
• Novel mutation 100%
• Or Comparative 20%
• Patient Information 20%
• Polymorphism 20%
• Population Analysis 20%
• Sequence Alignment 20%
• SLC40A1 100%
• TfR2 100%

Biochemistry, Genetics and Molecular Biology

• Ferroportin 33%
• Gene Sequence 33%
• Hemojuvelin 33%
• Hepcidin 33%
• Human Amniotic Membrane Powder 33%
• Iron Overload 33%
• Iron Poisoning 33%
• Missense Mutation 33%
• Sequence Alignment 33%
• Transferrin Receptor 100%

Medicine and Dentistry

• Clinical Feature 16%
• Disease 16%
• Ferroportin 16%
• Gene Sequence 16%
• Hemochromatosis 100%
• Hemojuvelin 16%
• Hepcidin 16%
• Iron Overload 16%
• Missense Mutation 16%
• Sequence Alignment 16%
• Transferrin Receptor 2 100%