The Incidence of Rett Syndrome in France-Reference-Cited by-同舟云学术

The Incidence of Rett Syndrome in France

Published:2006-05 Issue:5 Volume:34 Page:372-375
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Bienvenu Thierry,Philippe Christophe,De Roux Nicolas,Raynaud Martine,Bonnefond Jean Paul,Pasquier Laurent,Lesca Gaetan,Mancini Josette,Jonveaux Philippe,Moncla Anne,Feingold Josué,Chelly Jamel,Villard Laurent

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference23 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

2. Mutations and polymorphisms in the human methyl CpG-binding protein MECP2;Miltenberger-Miltenyi;Hum Mutat,2003

3. Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome;Laccone;Hum Mutat,2004

4. Gross rearrangements in the MECP2 gene in three patients with Rett syndrome;Schollen;Hum Mutat,2003

5. A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome;Mnatzakanian;Nat Genet,2004

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