Løvlie, R <br/><br/>
The Ca(2+)-sensing receptor gene (PCAR1) mutation T151M in isolated autosomal dominant hypoparathyroidism.  [electronic resource] 

 -  Human genetics  Aug 1996 
 - 129-33 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050174  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 3--genetics<br/>DNA, Complementary--genetics<br/>Female<br/>Genes, Dominant<br/>Genetic Linkage<br/>Genetic Markers<br/>Humans<br/>Hypoparathyroidism--genetics<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Pedigree<br/>Point Mutation<br/>Polymorphism, Single-Stranded Conformational<br/>Receptors, Calcium-Sensing<br/>Receptors, Cell Surface--genetics