Li, Dong <br/><br/>
Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Sep 2014 
 - E1774-83 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>1945-7197 
<br/><br/><label>Standard No.: </label>10.1210/jc.2014-1029  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Bone Development--genetics<br/>Child<br/>Child, Preschool<br/>Family Health<br/>Female<br/>GTP-Binding Protein alpha Subunits--genetics<br/>Genome-Wide Association Study<br/>Germ-Line Mutation--genetics<br/>Heterozygote<br/>Humans<br/>Hypercalciuria--genetics<br/>Hypocalcemia--genetics<br/>Hypoparathyroidism--congenital<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Phenotype<br/>Young Adult