Beaman, Glenda M <br/><br/>
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.  [electronic resource] 

 -  Clinical genetics  12 2019 
 - 515-520 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13631  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Family<br/>Female<br/>Homozygote<br/>Humans<br/>Malaysia<br/>Male<br/>Mutation, Missense--genetics<br/>Receptor, Muscarinic M3--genetics<br/>Urinary Bladder Diseases--genetics