Gorvin, Caroline M <br/><br/>
A G-protein Subunit-α11 Loss-of-Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2).  [electronic resource] 

 -  Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research  06 2016 
 - 1200-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1523-4681 
<br/><br/><label>Standard No.: </label>10.1002/jbmr.2778  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amino Acid Substitution<br/>Calcium Signaling--genetics<br/>Female<br/>Fibroblast Growth Factor-23<br/>GTP-Binding Protein alpha Subunits--chemistry<br/>HEK293 Cells<br/>Humans<br/>Hypercalcemia--genetics<br/>Mutation, Missense<br/>Protein Domains<br/>Receptors, Calcium-Sensing--genetics