D.R. Repaske
Division of Endocrinology
Children's Hospital Medical Center
Cincinnati
Ohio 45229-3039
USA
Name/email consistency: high
- 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. Repaske, D.R., Medlej, R., Gültekin, E.K., Krishnamani, M.R., Halaby, G., Findling, J.W., Phillips, J.A. J. Clin. Endocrinol. Metab. (1997)