Phenotypic manifestations ofMECP2 mutations in classical and atypical rett syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference55 articles.
1. Diagnostic criteria for rett syndrome
2. Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
4. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
5. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations
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