figure9

Figure 9. Schematic diagram of the Vasopressin-neurophysin II gene and its product, showing the location and type of mutations identified in autosomal dominant familial hypothalamic diabetes insipidus. Though mutations have been described in all three exons, and involve all parts of the VP-NPII precursor except the co-peptin moiety, the majority occur in exons 1or 2.

Figure 9. Schematic diagram of the Vasopressin-neurophysin II gene and its product, showing the location and type of mutations identified in autosomal dominant familial hypothalamic diabetes insipidus. Though mutations have been described in all three exons, and involve all parts of the VP-NPII precursor except the co-peptin moiety, the majority occur in exons 1or 2.

Figure 9. Schematic diagram of the Vasopressin-neurophysin II gene and its product, showing the location and type of mutations identified in autosomal dominant familial hypothalamic diabetes insipidus. Though mutations have been described in all three exons, and involve all parts of the VP-NPII precursor except the co-peptin moiety, the majority occur in exons 1or 2.