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October 1, 1995Journal of Clinical InvestigationOpen Access

Binding-, intracellular transport-, and biosynthesis-defective mutants of vasopressin type 2 receptor in patients with X-linked nephrogenic diabetes insipidus.

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Authors

HTHiroyasu TsukaguchiKansai Medical UniversityHMHiroaki MatsubaraUniversity of Notre DameSTShigeru TaketaniKansai Medical University

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Cite This Study

Tsukaguchi et al. (1995) studied this question.

synapsesocial.com/papers/6a880283dd9075da50bbeed0https://doi.org/10.1172/jci118252
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1The effect of eight V2 vasopressin receptor mutations on stimulation of adenylyl cyclase and binding to vasopressin.1994 · 84 citations
  2. 2Subtype-specific differences in the intracellular sorting of G protein-coupled receptors.1993 · 155 citations
  3. 3Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidus1994 · 19 citations