Weber, Stefanie <br/><br/>
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.  [electronic resource] 

 -  American journal of human genetics  Nov 2011 
 - 668-74 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2011.10.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Consanguinity<br/>Female<br/>Frameshift Mutation--genetics<br/>Humans<br/>INDEL Mutation--genetics<br/>Immunohistochemistry<br/>Male<br/>Metabolism, Inborn Errors--genetics<br/>Mice<br/>Mice, Knockout<br/>Models, Molecular<br/>Prune Belly Syndrome--genetics<br/>Receptor, Muscarinic M3--deficiency<br/>Sequence Homology, Nucleic Acid<br/>Sex Factors<br/>Urinary Bladder--embryology<br/>Urinary Bladder Neck Obstruction--genetics