Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males-Reference-Cited by-同舟云学术

Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males

Published:2007-06 Issue:5 Volume:29 Page:293-297
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Campos Mário,Abdalla Cláudia Bueno,Santos-Rebouças Cíntia Barros,dos Santos Adriana Vaz,Pestana Cristiane Pinheiro,Domingues Mariana Lopes,dos Santos Jussara Mendonça,Pimentel Márcia Mattos Gonçalves

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference38 articles.

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2. X-linked mental retardation;Ropers;Nat Rev Genet,2005

3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

4. Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype–genotype correlations;Amir;Am J Med Genet,2000

5. Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome;Lam;J Med Genet,2000

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1. MECP2-related conditions in males: A systematic literature review and 8 additional cases;European Journal of Paediatric Neurology;2021-09

2. Network Profiling of Brain-Expressed X-Chromosomal MicroRNA Genes Implicates Shared Key MicroRNAs in Intellectual Disability;Journal of Molecular Neuroscience;2019-01-03

3. Males With MECP2 C-terminal-Related Atypical Rett Syndromes and Their Carrier Mothers;Pediatric Neurology;2017-02

4. TheMECP2variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome;Clinical Genetics;2016-04-08

5. Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays;Pediatrics;2014-09-01