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Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.
Repaske, D R, Summar, M L, Krishnamani, M R, Gültekin, E K, Arriazu, M C, Roubicek, M E, Blanco, M, Isaac, G B, Phillips, J AVolume:
81
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.81.6.8964872
Date:
June, 1996
File:
PDF, 1.16 MB
english, 1996