Das, Dhanjit Kumar <br/><br/>
Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome.  [electronic resource] 

 -  Gene  Mar 2014 
 - 109-12 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-0038 
<br/><br/><label>Standard No.: </label>10.1016/j.gene.2013.12.063  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Child<br/>Female<br/>Forkhead Transcription Factors--chemistry<br/>Frameshift Mutation<br/>Humans<br/>India<br/>Methyl-CpG-Binding Protein 2--genetics<br/>Molecular Sequence Data<br/>Nerve Tissue Proteins--chemistry<br/>Protein Serine-Threonine Kinases--genetics<br/>Rett Syndrome--diagnosis<br/>Sequence Homology, Amino Acid