Characterization of the MeCP2R168X knockin mouse model for Rett syndrome.

PLoS One · 2014 · PMC4277341 · PMID 25541993

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failed to reach statistical significanceno p-value reported

General appearance of MeCP2 R168X/x mice Similar to their male mutant littermates MeCP2 deficient females had a lower body weight than the wild type mice but this difference failed to reach statistical significance ( Fig. 2A ).

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