Studies Show Key Steps of How Mutations to the MeCP2 Gene Cause Rett Syndrome

Published June 16, 2013 in Nature Neuroscience

Two collaborative papers reveal the key steps of how mutations to the MeCP2 gene cause Rett Syndrome by impairing the interaction between MeCP2 and the NCoR/SMRT co-repressor.

http://www.ncbi.nlm.nih.gov/pubmed/23770565

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