Fig. 3From: MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolutionMaximum likelihood topology based on MECP2 intron 3. Values above the nodes indicate the aLRT support estimates. Values below nodes indicate the posterior probabilities of the Bayesian tree and bootstrap estimates. Red circles indicate Alu insertionsBack to article page