Phenotypic Expression of CFH Rare Variants in Age-Related Macular Degeneration Patients in the Coimbra Eye Study.

13 , 15 , 16 Our results also suggest that the AMD phenotype characterized by thinner choroid and SDD seems to be more common in carriers of rare CFH variants, namely the association of SDD with the P258L variant, as well as having MNV in late stages, although these differences did not reach statistical significance in our analyzed population.

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