Liu, Hua <br/><br/>
HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.  [electronic resource] 

 -  European journal of medical genetics  Sep 2019 
 - 103540 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2018.09.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Basic Helix-Loop-Helix Transcription Factors--genetics<br/>Cardiomyopathy, Dilated--genetics<br/>Female<br/>HEK293 Cells<br/>HeLa Cells<br/>Heterozygote<br/>Humans<br/>Loss of Function Mutation<br/>Male<br/>Middle Aged<br/>Penetrance