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• 17:01, 14 June 2016 TheEmbroideryWarehouse talk contribs deleted page A situation was noted in human that carried mutations in pde6b and gpr98 genes that elevated the severity of the phenotypes when compared with siblings who were homozygous for only one particular of the two genes (Spam: content was: "In contrast, the photoreceptor degeneration in the Ush2a knockout mice is slowly progressive up to the age of 20 months exactly where much more than 50 percent of..." (and the only contributor was "[[Special:Contributions/Zoo7cap|Zo...)