Mutations in the transcriptional regulator MeCP2 severely impact key cellular and molecular signatures of human astrocytes during maturation
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference97 articles.
1. Identification of MeCP2 mutations in a series of females with autistic disorder;Carney;Pediatr. Neurol.,2003
2. MECP2 mutation in a boy with language disorder and schizophrenia;Cohen;Am. J. Psychiatry,2002
3. The story of Rett syndrome: from clinic to neurobiology;Chahrour;Neuron,2007
4. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
5. Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology;Ballas;Nat. Neurosci.,2009
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