V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms

Human Mutation

Volumn 12, Issue 3, 1998, Pages 196-205

  Schöneberg, Torsten ^a   Schulz, Angela ^a   Biebermann, Heike ^b   Grüters, Anette ^b   Grimm, Torsten ^c   Hübschmann, Klaus ^c   Filler, Guido ^b   Gudermann, Thomas ^a   Schultz, Günter ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

^b HUMBOLDT UNIVERSITY   (Germany)

^c KLINIKUM ERNST VON BERGMANN   (Germany)

Author keywords

Nephrogenic diabetes insipidus; Protein folding; Protein trafficking; Receptor mutations; Vasopressin receptor

Indexed keywords

VASOPRESSIN RECEPTOR;

ARTICLE; CASE REPORT; CHILD; ENZYME ACTIVATION; ENZYME LINKED IMMUNOSORBENT ASSAY; GENE MUTATION; GENETIC ANALYSIS; HUMAN; NEPHROGENIC DIABETES INSIPIDUS; PRIORITY JOURNAL; PROTEIN EXPRESSION; RECEPTOR AFFINITY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; COS CELLS; DIABETES INSIPIDUS, NEPHROGENIC; DNA; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; RECEPTORS, VASOPRESSIN; X CHROMOSOME;

EID: 0031903345     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1998)12:3<196::AID-HUMU7>3.0.CO;2-F     Document Type: Article

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