Associations betweenmeCP2 mutations, x-chromosome inactivation, and phenotype-Reference-Cited by-同舟云学术

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Associations betweenmeCP2 mutations, x-chromosome inactivation, and phenotype

Published:2002 Issue:2 Volume:8 Page:99-105
ISSN:1080-4013
Container-title:Mental Retardation and Developmental Disabilities Research Reviews
language:en
Short-container-title:Ment. Retard. Dev. Disabil. Res. Rev.

Author:

Hoffbuhr K. C.,Moses L. M.,Jerdonek M. A.,Naidu S.,Hoffman E. P.

Publisher

Wiley

Subject

Genetics(clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology, and Child Health

Reference50 articles.

1. Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

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

3. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

4. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations

5. MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features

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