DOI:
10.1055/s-00000017
Experimental and Clinical Endocrinology & Diabetes
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References
Repaske DR, Medlej R, Gültekin EK, Krishnamani MRS, Halaby G, Findling JW, Phillips JA.
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.
J Clin Endocrinol Metab. 82: 51-56 1997;
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