Lee, S S <br/><br/>
Spectrum of MECP2 mutations in Rett syndrome.  [electronic resource] 

 -  Brain & development  Dec 2001 
 - S138-43 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0387-7604 
<br/><br/><label>Standard No.: </label>10.1016/s0387-7604(01)00339-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Base Sequence--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomal Proteins, Non-Histone<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Frameshift Mutation--genetics<br/>Genetic Testing<br/>Humans<br/>Male<br/>Methyl-CpG-Binding Protein 2<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Repressor Proteins<br/>Rett Syndrome--genetics