![](/img/cover-not-exists.png)
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 1
Repaske, David R., Medlej, Rita, Gültekin, Ebrû K., Krishnamani, M. R. S., Halaby, George, Findling, James W., Phillips, John A.Volume:
82
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.82.1.3660
Date:
January, 1997
File:
PDF, 2.34 MB
english, 1997