Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome

Keyphrases

• Gene mutation 100%
• Autosomal Recessive 100%
• Atypical Hemolytic Uremic Syndrome (aHUS) 100%
• Complement Factor H 100%
• Complement Factor H Gene 100%
• Kindred 60%
• Functional Analysis 40%
• Bedouin 40%
• Early Onset 40%
• Hypertension 20%
• Linkage Analysis 20%
• Acute Renal Failure 20%
• Missense mutation 20%
• Nuclear Family 20%
• Genetic Analysis 20%
• Clinical Features 20%
• Mode of Inheritance 20%
• Mutation Analysis 20%
• Consanguineous 20%
• Affected children 20%
• Coding Region 20%
• Complement System 20%
• Microangiopathic Hemolytic Anemia 20%
• Factor H mutation 20%
• Complement Components 20%
• Hypocomplementemia 20%
• Chromosome 1q 20%
• Intracellular Trafficking 20%
• H Protein 20%
• Regulatory Component 20%

Medicine and Dentistry

• Gene Mutation 100%
• Autosomal Recessive Inheritance 100%
• Complement Factor H 100%
• Atypical Hemolytic Uremic Syndrome 100%
• Disease 25%
• Acute Kidney Injury 12%
• Secretion (Process) 12%
• Clinical Feature 12%
• Linkage Analysis 12%
• Gene Linkage 12%
• Complement System 12%
• Missense Mutation 12%
• Thrombotic Thrombocytopenic Purpura 12%
• Intracellular Trafficking 12%
• Hypocomplementemia 12%
• Chromosome 1q 12%

Biochemistry, Genetics and Molecular Biology

• Gene Mutation 100%
• Autosomal Recessive Inheritance 100%
• Factor H 100%
• Genetics 12%
• Secretion (Process) 12%
• Missense Mutation 12%
• Linkage Analysis 12%
• Gene Linkage 12%
• Coding Region 12%
• Thrombotic Thrombocytopenic Purpura 12%
• Complement System 12%
• Chromosome 1q 12%
• Intracellular Trafficking 12%