Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference28 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. Rett syndrome: update of a 25 year follow-up investigation in Western Sweden – sociomedical aspects
3. The Methyl-CpG Binding Transcriptional Repressor MeCP2 Stably Associates with Nucleosomal DNA
4. Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location
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