Rajaei, Saideh <br/><br/>
Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.  [electronic resource] 

 -  Journal of child neurology  Jan 2011 
 - 65-71 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1708-8283 
<br/><br/><label>Standard No.: </label>10.1177/0883073810374125  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Angelman Syndrome--genetics<br/>Child<br/>Child, Preschool<br/>Chromatography, High Pressure Liquid<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Infant<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Mutation<br/>Polymerase Chain Reaction<br/>Protein Serine-Threonine Kinases--genetics<br/>Rett Syndrome--diagnosis<br/>Sweden