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Pandora MSCA ITN consortium to investigate how Chromosome 1 (Chr1) AMD risk variants—including the complement factor H CFH Y402H polymorphism—drive intrinsic defects and cell death in photoreceptors, and
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, methylation, whole genome sequencing and single nucleotide polymorphism (SNP) and spatial data. This cancer is a rare disease that has not yet been documented and we believe that these data will be a major
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