Barely Significant
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Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina.

Front Mol Biosci · 2021 · PMC8360850 · PMID 34395527

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In this regard, although we could observe a slight increase in the specific activity of Q90E in the presence of PN and of R271K in the presence of PN or PM, the differences did not reach statistical significance ( Figure 5B ).

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