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VAN DEN VEYVER, IGNATIA
One or more keywords matched the following items that are connected to
VAN DEN VEYVER, IGNATIA
Item Type
Name
Academic Article
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
Academic Article
Methyl-CpG-binding protein 2 mutations in Rett syndrome.
Academic Article
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.
Academic Article
Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome.
Academic Article
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.
Academic Article
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.
Academic Article
Genetic basis of Rett syndrome.
Academic Article
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.
Academic Article
Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.
Academic Article
Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.
Concept
Rett Syndrome
Grant
Pathophysiology of Rett Syndrome /MECP2 Mutations
Search Criteria
Rett Syndrome