Barely Significant
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Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.

Sci Rep · 2019 · PMC6609610 · PMID 31273259

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failed to reach significanceno p-value reported
Expression level differences between patients, however, led to standard error values, that failed to reach significance when values from the three corneas were pooled.

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