Breaking the silence in Rett syndrome
- PMID: 10508498
- DOI: 10.1038/13751
Breaking the silence in Rett syndrome
Comment on
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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.Nat Genet. 1999 Oct;23(2):185-8. doi: 10.1038/13810. Nat Genet. 1999. PMID: 10508514
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