Updating the profile of C-terminal MECP2 deletions in Rett syndrome

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Phenotypic manifestations of MECP2 mutations in classical and atypical rett syndrome2003 · 123 citations
2. 2Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation2006 · 110 citations
3. 3Investigating genotype–phenotype relationships in Rett syndrome using an international data set2008 · 244 citations
4. 4Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?2003 · 85 citations
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