Barely Significant
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The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation.

Mol Vis · 2015 · PMC4663191 · PMID 26664249

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highly significantp<0.0001actually significant
The TUNEL counts for the Grk1 −/− ;B6J mice were also highly significant compared to the B6J and B6N mice in the 1-month-old superior retinas (****p<0.0001) but were less significant for the 1- and 3-month-old inferior retinas (***p<0.001) and the 3-month-old superior retinas (**p<0.01).

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