Rett Syndrome and the Impact of MeCP2 Associated Transcriptional Mechanisms on Neurotransmission
Author:
Publisher
Elsevier BV
Subject
Biological Psychiatry
Reference76 articles.
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2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
3. Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations;Amir;Am J Med Genet,2000
4. MECP2 mutations account for most cases of typical forms of Rett syndrome;Bienvenu;Hum Mol Genet,2000
5. Rett syndrome: Analysis of MECP2 and clinical characterization of 31 patients;Huppke;Hum Mol Genet,2000
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