Houweling, Arjan C <br/><br/>
Loss-of-function variants in myocardin cause congenital megabladder in humans and mice.  [electronic resource] 

 -  The Journal of clinical investigation  12 2019 
 - 5374-5380 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>1558-8238 
<br/><br/><label>Standard No.: </label>10.1172/JCI128545  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Animals<br/>Female<br/>Genetic Variation<br/>Humans<br/>Male<br/>Mice<br/>Muscle, Smooth--metabolism<br/>Mutation<br/>Nuclear Proteins--genetics<br/>Trans-Activators--genetics<br/>Urinary Bladder--abnormalities