DOI:
10.1055/s-00000017
Experimental and Clinical Endocrinology & Diabetes
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References
Rutishauser J, Böni-Schnetzler M, Böni J, Wichmann W, Huisman T, Vallotton MB, Froesch ER.
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.
J Clin Endocrinol Metab. 81: 92-198 1996;
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