Barely Significant
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The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.

Hum Mol Genet · 2016 · PMC4731022 · PMID 26647311

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In cases where differences between mutant and WT-GFP mice did not reach statistical significance (R133C and R306C in the elevated plus maze, and T158M on the hanging-wire test), the data showed trends towards defective performance that matched those detected in the comparison with littermates.

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