DOI:
10.1055/s-00000025
Hormone and Metabolic Research
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References
Fluck CE, Deladoey J, Nayak S. et al.
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused
by a novel mutation (C59Delta/A60W) in the neurophysin moiety of
prepro-vasopressin-neurophysin II (AVP-NP II).
Eur J Endocrinol 2001;
145: 439-444
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