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Introduction: Rett syndrome.

作者信息

Zoghbi Huda Y

机构信息

Department of Pediatrics, Molecular and Human Genetics, Neuroscience, and Neurology, Baylor College of Medicine, Houston, Texas, 77030, USA.

出版信息

Ment Retard Dev Disabil Res Rev. 2002;8(2):59-60. doi: 10.1002/mrdd.10028.

DOI:10.1002/mrdd.10028

PMID:12112727

Abstract

摘要

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Introduction: Rett syndrome.

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Breaking the silence in Rett syndrome.

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引用本文的文献

How do immune cells support and shape the brain in health, disease, and aging?

J Neurosci. 2013 Nov 6;33(45):17587-96. doi: 10.1523/JNEUROSCI.3241-13.2013.

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相似文献

Introduction: Rett syndrome.

Ment Retard Dev Disabil Res Rev. 2002;8(2):59-60. doi: 10.1002/mrdd.10028.

Breaking the silence in Rett syndrome.

Nat Genet. 1999 Oct;23(2):127-8. doi: 10.1038/13751.

[Rett syndrome].

Ryoikibetsu Shokogun Shirizu. 2000(30 Pt 5):228-30.

Discovery of the Rett syndrome gene and its function.

Turk J Pediatr. 2000 Oct-Dec;42(4):271.

[First gene connected to autism spectrum disorders has been found].

Duodecim. 2000;116(20):2185-7.

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.

Curr Top Dev Biol. 2004;59:61-86. doi: 10.1016/S0070-2153(04)59003-8.

Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome.

Clin Genet. 2005 Jun;67(6):532-3. doi: 10.1111/j.1399-0004.2005.00444.x.

[Clinical and molecular genetic findings in four girls with Rett syndrome].

Klin Padiatr. 2002 Sep-Oct;214(5):291-4. doi: 10.1055/s-2002-34016.

Genetic basis of Rett syndrome.

Ment Retard Dev Disabil Res Rev. 2002;8(2):82-6. doi: 10.1002/mrdd.10025.

Another patient with MECP2 mutation without classic Rett syndrome phenotype.

Pediatr Neurol. 2005 May;32(5):355-7. doi: 10.1016/j.pediatrneurol.2004.12.012.

引用本文的文献

How do immune cells support and shape the brain in health, disease, and aging?

J Neurosci. 2013 Nov 6;33(45):17587-96. doi: 10.1523/JNEUROSCI.3241-13.2013.

Introduction: Rett syndrome.

作者信息

机构信息

出版信息

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Introduction: Rett syndrome.

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