Zhang, Min <br/><br/>
MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.  [electronic resource] 

 -  Molecular medicine reports  Sep 2017 
 - 2747-2754 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1791-3004 
<br/><br/><label>Standard No.: </label>10.3892/mmr.2017.6875  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Animals<br/>Basic Helix-Loop-Helix Transcription Factors--chemistry<br/>Child<br/>Child, Preschool<br/>Double Outlet Right Ventricle--genetics<br/>Female<br/>HEK293 Cells<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation, Missense<br/>Sequence Alignment<br/>Transcriptional Activation<br/>Young Adult