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13810
13810
https://scigraph.springernature.com/pub.10.1038/13810
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
P2888
Q22337290-64EDE35B-46FD-416F-9B3C-0AA6BDB0E64E
P2888
13810
https://scigraph.springernature.com/pub.10.1038/13810