MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders-Reference-Cited by-同舟云学术

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MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders

Published:2012-06 Issue:6 Volume:34 Page:487-495
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Psoni Stavroula,Sofocleous Christalena,Traeger-Synodinos Joanne,Kitsiou-Tzeli Sophia,Kanavakis Emmanuel,Fryssira-Kanioura Helen

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2 encoding methyl-CpG-binding protein2;Amir;Nat Genet,1999

2. Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS;Hitchins;Am J Med Genet,2004

3. MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype–genotype correlation;Gomot;Am J Med Genet A,2003

4. Recent advances in MeCP2 structure and function;Hite;Biochem Cell Biol,2009

5. DNA methylation-related chromatin remodelling in activity-dependent BDNF gene regulation;Martinowich;Science,2003

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Instability and Disease Progression of Indian Rett Syndrome Patients;Molecular Neurobiology;2023-12-26

2. R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report;Clinical Pathology;2022-01

3. Movement disorders in patients with R ett syndrome: A systematic review of evidence and associated clinical considerations;Psychiatry and Clinical Neurosciences;2021-10-21

4. Rett Syndrome as a movement and motor disorder – A narrative review;European Journal of Paediatric Neurology;2020-09

5. Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways;OMICS: A Journal of Integrative Biology;2020-03-01

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