A Mutation in the Rett Syndrome Gene, MECP2, Causes X-Linked Mental Retardation and Progressive Spasticity in Males
- 1 October 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (4), 982-985
- https://doi.org/10.1086/303078
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Methyl-CpG-binding protein 2 mutations in Rett syndromeCurrent Opinion in Genetics & Development, 2000
- Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.Human Molecular Genetics, 2000
- MECP2 mutations account for most cases of typical forms of Rett syndromeHuman Molecular Genetics, 2000
- Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypesAnnals of Neurology, 2000
- Preserved speech variant is allelic of classic Rett syndromeEuropean Journal of Human Genetics, 2000
- Mutation screening in Rett syndrome patientsJournal of Medical Genetics, 2000
- Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG HotspotsAmerican Journal of Human Genetics, 1999
- The Methyl-CpG Binding Transcriptional Repressor MeCP2 Stably Associates with Nucleosomal DNABiochemistry, 1999
- A novel X-linked gene, G4.5. is responsible for Barth syndromeNature Genetics, 1996
- Human Brain Factor 1, a New Member of the Fork Head Gene FamilyGenomics, 1994