Pitcher, Meagan R <br/><br/>
Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene.  [electronic resource] 

 -  Human molecular genetics  May 2015 
 - 2662-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddv030  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Substitution<br/>Animals<br/>Behavior, Animal<br/>Disease Models, Animal<br/>Fibroblasts--drug effects<br/>Gene Expression<br/>Genetic Association Studies<br/>Gentamicins--pharmacology<br/>Mechanistic Target of Rapamycin Complex 1<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Mice<br/>Mice, Transgenic<br/>Multiprotein Complexes--metabolism<br/>Mutation<br/>Phenotype<br/>RNA, Messenger--genetics<br/>Rett Syndrome--diagnosis<br/>Signal Transduction<br/>TOR Serine-Threonine Kinases--metabolism<br/>Transgenes