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Article

Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent

28 Jun 2010

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20581873
DOI: 10.1038/ng0710-553

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Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independentPMID 20581873Read ↗

Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.Semantic proximity Read ↗

Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.Semantic proximity Read ↗

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.Semantic proximity Read ↗

Contribution of copy number variation in the regulation of complement activation locus to development of age-related macular degeneration.Semantic proximity Read ↗

Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10.Semantic proximity Read ↗

Genetic Polymorphisms of CFH and ARMS2 Do Not Predict Response to Antioxidants and Zinc in Patients with Age-Related Macular Degeneration: Independent Statistical Evaluations of Data from the Age-Related Eye Disease Study.Semantic proximity Read ↗

The SERPING1 gene and age-related macular degeneration.Semantic proximity Read ↗

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications.Semantic proximity Read ↗

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