Respiratory and sleep disorders in female children with atypical Rett syndrome caused by mutations in theCDKL5gene
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2012.04432.x/fullpdf
Reference17 articles.
1. Rett syndrome: revised diagnostic criteria and nomenclature;Neul;Ann Neurol,2010
2. Disturbances in cardiorespiratory function during day and night in Rett syndrome;Rohdin;Pediatr Neurol,2007
3. Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome;Neul;Neurology,2008
4. Mutations in CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation;Weaving;Am J Hum Genet,2004
5. Key clinical features to identify girls with CDKL5 mutations;Bahi-Buisson;Brain,2008
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