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Neuroscience|March 15, 2014
Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168XJ M Bissonnette, L R Schaevitz, S J Knopp, et al.
Genes, Brain, and Behavior|November 29, 2013
MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficitsL R Schaevitz, N B Gómez, D P Zhen, et al.
Neuroscience|March 27, 2007
Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndromeN A Stearns, L R Schaevitz, H Bowling, et al.
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