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First published 2011-5

Analysis of MECP2 Gene Copy Number in Boys With Autism

Chun-Yan Xi, Yao Lu, Ying-Hua Tan [...]

Journal of Child Neurology

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First published 2010-8

Mutational Analysis of the MECP2 Gene in Tunisian Patients With Rett Syndrome: A Novel Double Mutation

Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Dorsaf Moalla [...]

Journal of Child Neurology

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Research article

First published 2009-02

A Novel MECP2 Gene Mutation in a Tunisian Patient with Rett Syndrome

Nourhène Fendri-Kriaa, Zaineb Abdelkafi, Imen Ben Rebeh [...]

Genetic Testing and Molecular Biomarkers

Open access

Case report

First published 2018-4-13

When Rett syndrome is due to genes other than MECP2

Alan K. Percy, Jane Lane, Fran Annese [...]

Translational Science of Rare Diseases

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Research article

First published 2008-09

Multiple De Novo Mutations in the MECP2 Gene

David J. Bunyan, David O. Robinson

Genetic Testing and Molecular Biomarkers

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First published 2004-07

Influence of MECP2 Gene Mutation and X-Chromosome Inactivation on the Rett Syndrome Phenotype

Jong Hee Chae, Hee Hwang, Yong Seung Hwang [...]

Journal of Child Neurology

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First published 2009-1

Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients

Mónica Santos, Teresa Temudo, Teresa Kay [...]

Journal of Child Neurology

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Review article

First published 2012-3

Algorithmic Approach for Methyl-CpG Binding Protein 2 ( MECP2 ) Gene Testing in Patients With Neurodevelopmental Disabilities

Jennifer N. Sanmann, G. Bradley Schaefer, Bruce A. Buehler [...]

Journal of Child Neurology

Open access

Case report

First published 2022

R306X Mutation in the MECP2 Gene Causes an Atypical Rett Syndrome in a Moroccan Patient: A Case Report

Wafaa Bouzroud, Amal Tazzite, Sarah Berrada [...]

Sage Open Pathology

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Research article

First published 2012-5

Novel Mutations in the C-Terminal Region of the MECP2 Gene in Tunisian Rett Syndrome Patients

Nourhene Fendri-Kriaa, Aida Rouissi, Rania Ghorbel [...]

Journal of Child Neurology

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