Kamperis, K <br/><br/>
A novel splicing mutation in the V2 vasopressin receptor.  [electronic resource] 

 -  Pediatric nephrology (Berlin, Germany)  Nov 2000 
 - 43-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0931-041X 
<br/><br/><label>Standard No.: </label>10.1007/s004670000431  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing<br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Base Sequence<br/>Child, Preschool<br/>Deamino Arginine Vasopressin<br/>Denmark<br/>Diabetes Insipidus, Nephrogenic--diagnosis<br/>Female<br/>Genomic Imprinting<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Pedigree<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Protein Structure, Secondary<br/>Receptors, Vasopressin--chemistry<br/>X Chromosome