Nephrogenic diabetes insipidus caused by mutation of Tyr205: a key residue of V2 vasopressin receptor function.

Human mutation

Volumn 25, Issue 5, 2005, Pages 505-

  Sangkuhl, Katrin ^a   Römpler, Holger ^a   Busch, Wibke ^a   Karges, Beate ^a   Schöneberg, Torsten ^a  

^a UNIVERSITY OF LEIPZIG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TYROSINE; VASOPRESSIN RECEPTOR;

ADULT; AMINO ACID SEQUENCE; ARTICLE; CASE REPORT; CHEMISTRY; FEMALE; GENETICS; HUMAN; INFANT; MALE; MISSENSE MUTATION; MOLECULAR EVOLUTION; MOLECULAR GENETICS; NEPHROGENIC DIABETES INSIPIDUS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHYSIOLOGY; PROTEIN TERTIARY STRUCTURE;

ADULT; AMINO ACID SEQUENCE; CONSERVED SEQUENCE; DIABETES INSIPIDUS, NEPHROGENIC; EVOLUTION, MOLECULAR; FEMALE; HUMANS; INFANT; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PEDIGREE; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, VASOPRESSIN; TYROSINE;

MLCS; MLOWN;

EID: 33744524097     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9337     Document Type: Article

References (0)