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      Heterogeneity in Clinical Manifestation of Autosomal Dominant Neurohypophyseal Diabetes Insipidus Caused by a Mutation Encoding Ala-1->Val in the Signal Peptide of the Arginine Vasopressin/Neurophysin II/Copeptin Precursor

      Journal of Clinical Endocrinology & Metabolism
      The Endocrine Society

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          Journal
          Journal of Clinical Endocrinology & Metabolism
          Journal of Clinical Endocrinology & Metabolism
          The Endocrine Society
          0021-972X
          January 01 1997
          January 01 1997
          : 82
          : 1
          : 51-56
          Article
          10.1210/jc.82.1.51
          2bc2b68a-2908-4eab-9d65-cb0747f5b037
          © 1997
          History

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