Classic rett syndrome in a boy as a result of somatic mosaicism for a mecp2 mutation
- 25 October 2001
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 50 (5) , 692
- https://doi.org/10.1002/ana.1272
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- MeCP2 mutations in children with and without the phenotype of Rett syndromeNeurology, 2001
- MECP2 is highly mutated in X-linked mental retardationHuman Molecular Genetics, 2001
- Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding proteinJournal of Medical Genetics, 2001
- Two affected boys in a Rett syndrome familyNeurology, 2000
- Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG HotspotsAmerican Journal of Human Genetics, 1999