Melo, Maria Edna de <br/><br/>
Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel mutation in arginine-vasopressin gene in a Brazilian family.  [electronic resource] 

 -  Arquivos brasileiros de endocrinologia e metabologia  Nov 2008 
 - 1272-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1677-9487 
<br/><br/><label>Standard No.: </label>10.1590/s0004-27302008000800011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acid Sequence<br/>Arginine Vasopressin--genetics<br/>Brazil<br/>Case-Control Studies<br/>Child<br/>Child, Preschool<br/>Diabetes Insipidus, Neurogenic--genetics<br/>Female<br/>Genes, Dominant--genetics<br/>Heterozygote<br/>Humans<br/>Middle Aged<br/>Mutation--genetics<br/>Pedigree<br/>Young Adult