Hébert, Betty <br/><br/>
Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule.  [electronic resource] 

 -  Orphanet journal of rare diseases  Aug 2014 
 - 124 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1750-1172 
<br/><br/><label>Standard No.: </label>10.1186/s13023-014-0124-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Fragile X Mental Retardation Protein--genetics<br/>Fragile X Syndrome--genetics<br/>Humans<br/>Large-Conductance Calcium-Activated Potassium Channel alpha Subunits--physiology<br/>Mice<br/>Mice, Knockout<br/>Phenotype