A Novel Mutation in the Vasopressin V2 Receptor Gene in a Woman with Congenital Nephrogenic Diabetes Insipidus

Internal Medicine

Volumn 38, Issue 10, 1999, Pages 808-812

  Sato, Kei ^a,b   Fukuno, Hiroshi ^a   Taniguchi, Tetsuzo ^a   Sawada, Seizo ^a   Fukui, Takafumi ^a   Kinoshita, Moritoshi ^a  

^a OTSUKA PHARMACEUTICAL CO LTD   (Japan)

^b Anan Central Hospital   (Japan)

Author keywords

Missense mutation; Polyuria; Vasopressin receptor

Indexed keywords

ARGIPRESSIN; URINARY TRACT AGENT; VASOPRESSIN RECEPTOR;

AMINO ACID SEQUENCE; ARTICLE; CASE REPORT; CHEMISTRY; DRUG RESISTANCE; FEMALE; FLUID THERAPY; GASTROINTESTINAL TUMOR; GENETICS; HUMAN; MIDDLE AGED; MISSENSE MUTATION; MOLECULAR GENETICS; NEPHROGENIC DIABETES INSIPIDUS; NUCLEOTIDE SEQUENCE;

AMINO ACID SEQUENCE; ARGININE VASOPRESSIN; BASE SEQUENCE; DIABETES INSIPIDUS, NEPHROGENIC; DRUG RESISTANCE; FEMALE; FLUID THERAPY; GASTROINTESTINAL NEOPLASMS; HUMANS; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; RECEPTORS, VASOPRESSIN; RENAL AGENTS;

EID: 0033209740     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.38.808     Document Type: Article

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