Genetic basis of rett syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology, and Child Health
Reference72 articles.
1. The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse
2. Rett syndrome: A search for gene sources
3. Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome
4. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
5. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
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