Molecular and cellular defects in nephrogenic diabetes insipidus

Current Opinion in Nephrology and Hypertension

Volumn 5, Issue 4, 1996, Pages 353-358

  Knoers, Nine V A M ^a   Van Os, Carel H ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AQUAPORIN; ARGIPRESSIN; COMPLEMENTARY DNA; VASOPRESSIN; VASOPRESSIN V2 RECEPTOR;

AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; GENE MUTATION; HETEROZYGOTE; HUMAN; NEPHROGENIC DIABETES INSIPIDUS; PRIORITY JOURNAL; REVIEW; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKED DISORDER;

AMINO ACID SEQUENCE; ANIMALS; AQUAPORIN 2; AQUAPORIN 6; AQUAPORINS; DIABETES INSIPIDUS, NEPHROGENIC; FEMALE; GENES, RECESSIVE; GENETIC COUNSELING; HETEROZYGOTE DETECTION; HUMANS; ION CHANNELS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN STRUCTURE, SECONDARY; RECEPTORS, VASOPRESSIN; X CHROMOSOME;

EID: 0029978973     PISSN: 10624821     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041552-199607000-00011     Document Type: Review

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