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In der Studie von Leyden et al

LCA10 is a severe form of retinal dystrophy caused by an adenine to guanine point mutation within intron 26 of the human CEP290 gene (IVS26)resulting in the inclusion of a cryptic exon and a premature stop codon [62]

Age impairs this process causing lipofuscin accumulation in RPE

1 They help clear damaged collagen while protecting the good stuff

Research Overview GHK-Cu is the copper(II) complex of the tripeptide glycyl-L-histidyl-L-lysine, a naturally occurring human sequence first isolated from plasma by Loren Pickart in 1973 and subsequently identified in saliva and urine

Often split into two injections: 250mcg fasted AM and 250mcg pre-bed