Pages that link to "Q38423796"
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The following pages link to Phenotypic Characterization of Complement Factor H R1210C Rare Genetic Variant in Age-Related Macular Degeneration (Q38423796):
Displaying 14 items.
- Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD. (Q36116190) (← links)
- Phenotype Characteristics of Patients With Age-Related Macular Degeneration Carrying a Rare Variant in the Complement Factor H Gene (Q38599697) (← links)
- Complement factor H in AMD: Bridging genetic associations and pathobiology. (Q46022690) (← links)
- Macular Degeneration Epidemiology: Nature-Nurture, Lifestyle Factors, Genetic Risk, and Gene-Environment Interactions - The Weisenfeld Award Lecture (Q47149024) (← links)
- Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration (Q47335501) (← links)
- Genetics and genetic testing for age-related macular degeneration. (Q48326680) (← links)
- Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation. (Q51213973) (← links)
- A Deep Phenotype Association Study Reveals Specific Phenotype Associations with Genetic Variants in Age-related Macular Degeneration: Age-Related Eye Disease Study 2 (AREDS2) Report No. 14. (Q52818918) (← links)
- Soft Drusen in Age-Related Macular Degeneration: Biology and Targeting Via the Oil Spill Strategies (Q57826004) (← links)
- Validated Prediction Models for Macular Degeneration Progression and Predictors of Visual Acuity Loss Identify High Risk Individuals (Q58589253) (← links)
- The ARMS2 A69S Polymorphism Is Associated with Delayed Rod-Mediated Dark Adaptation in Eyes at Risk for Incident Age-Related Macular Degeneration (Q58594328) (← links)
- Complement System and Age-Related Macular Degeneration: Implications of Gene-Environment Interaction for Preventive and Personalized Medicine (Q58702202) (← links)
- The Challenges and Promise of Complement Therapeutics for Ocular Diseases. (Q64905140) (← links)
- Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen (Q92579873) (← links)