People with MECP2 mutation-positive Rett disorder who converse-Reference-Cited by-同舟云学术

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People with MECP2 mutation-positive Rett disorder who converse

Published:2006-05 Issue:5 Volume:50 Page:386-394
ISSN:0964-2633
Container-title:Journal of Intellectual Disability Research
language:en
Short-container-title:J Intellect Disabil Res

Author:

Kerr A. M.,Archer H. L.,Evans J. C.,Prescott R. J.,Gibbon F.

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical),Neurology,Arts and Humanities (miscellaneous),Rehabilitation

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.2005.00786.x/fullpdf

Reference33 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

2. Neuropathology of Rett syndrome

3. Morphological study of neocortical areas in Rett syndrome

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1. Use of a low-tech tool in the improvement of social interaction of patients with Rett Syndrome: an observational study;Frontiers in Public Health;2024-04-04

2. To speak may draw on epigenetic writing and reading: Unravelling the complexity of speech and language outcomes across chromatin-related neurodevelopmental disorders;Neuroscience & Biobehavioral Reviews;2023-09

3. An overview of Rett syndrome;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

4. Regression in Rett syndrome: Developmental pathways to its onset;Neuroscience & Biobehavioral Reviews;2019-03

5. Brain X chromosome inactivation is not random and can protect from paternally inherited neurodevelopmental disease;2018-11-02

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