Monroy-Muņoz, Irma Eloisa <br/><br/>
Novel mutations in the transcriptional activator domain of the human TBX20 in patients with atrial septal defect.  [electronic resource] 

 -  BioMed research international  2015 
 - 718786 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2314-6141 
<br/><br/><label>Standard No.: </label>10.1155/2015/718786  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Animals<br/>Child<br/>Female<br/>Heart Septal Defects, Atrial--genetics<br/>Humans<br/>Male<br/>Mutation, Missense--genetics<br/>Organogenesis--genetics<br/>Protein Structure, Tertiary<br/>Sequence Analysis, DNA<br/>T-Box Domain Proteins--genetics<br/>Transcriptional Activation--genetics