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13810
13810
http://dx.doi.org/10.1038/13810
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
P356
Q22337290-6A67AA78-0E73-49C7-82BC-9E53190EA208
P356
13810
http://dx.doi.org/10.1038/13810