Vasopressin receptor mutations causing nephrogenic diabetes insipidus

Proceedings of the Association of American Physicians

Volumn 110, Issue 5, 1998, Pages 387-394

  Bichet, D G ^a   Turner, M ^a   Morin, D ^a  

^a HÔPITAL DU SACRÉ COEUR DE MONTRÉAL   (Canada)

Author keywords

Arginine vasopressin; Expression studies; Loss of function mutations; Prenatal testing; X linked disease

Indexed keywords

DESMOPRESSIN; VASOPRESSIN RECEPTOR;

BASOLATERAL MEMBRANE; CRYSTALLIZATION; GENE EXPRESSION REGULATION; GENE MUTATION; HETEROZYGOTE; HORMONE ACTION; HUMAN; MULTIGENE FAMILY; NEPHROGENIC DIABETES INSIPIDUS; PROTEIN DOMAIN; RECEPTOR GENE; REVIEW; VASOPRESSIN RELEASE; WATER PERMEABILITY;

AMINO ACID SEQUENCE; DIABETES INSIPIDUS, NEPHROGENIC; HETEROZYGOTE; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PRENATAL DIAGNOSIS; RECEPTORS, VASOPRESSIN;

EID: 0031690408     PISSN: 1081650X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (57)