A Novel Point Mutation in the Translation Initiation Codon of the Pre-Pro-Vasopressin-Neurophysin II Gene: Cosegregation with Morphological Abnormalities and Clinical Symptoms in Autosomal Dominant Neurohypophyseal Diabetes Insipidus

Jonas Rutishauser, Marianne Böni-Schnetzler, Jürg Böni, Werner Wichmann, Thierry Huisman, Michel B. Vallotton, E. Rudolf Froesch

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