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Articles (6)

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1-6 of 6 results for T158M

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

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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

Select article: Spectrum of MECP2 Mutations in Rett Syndrome

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Research article

First published 2002-03

Spectrum of MECP2 Mutations in Rett Syndrome

Thierry Bienvenu, Laurent Villard, Nicolas De Roux [...]

Genetic Testing and Molecular Biomarkers

Select article: Mutation Analysis of MECP2 and Clinical Characterization in Korean Patients With Rett Syndrome

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First published 2002-01

Mutation Analysis of MECP2 and Clinical Characterization in Korean Patients With Rett Syndrome

Jong Hee Chae, Yong Seung Hwang, Ki Joong Kim

Journal of Child Neurology

Select article: Occurrence of Rett Syndrome in Boys

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First published 2001-05

Occurrence of Rett Syndrome in Boys

Helen Leonard, Jon Silberstein, Rena Falk [...]

Journal of Child Neurology

Select article: Rett Syndrome: North American Database

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First published 2007-12

Rett Syndrome: North American Database

Alan K. Percy, Jane B. Lane, Jerry Childers [...]

Journal of Child Neurology

Select article: Rett Syndrome: Prevalence Among Chinese and a Comparison of MECP2 Mutations of Classic Rett Syndrome With Other Neurodevelopmental Disorders

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First published 2007-12

Rett Syndrome: Prevalence Among Chinese and a Comparison of MECP2 Mutations of Classic Rett Syndrome With Other Neurodevelopmental Disorders

Virginia C. N. Wong, Susanna Y. H. Li

Journal of Child Neurology

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