A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus
Ilhan, MAHMUT MUZAFFER
YILDIZ, R. S.
Tiryakioglu, N. O.
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Purpose Familial neurohypophyseal diabetes insipidus (FNDI) is a rare, autosomal dominant, inherited disorder which is characterized by severe polydipsia and polyuria generally presenting in early childhood. In the present study, we aimed to analyze the AVP gene in a Turkish family with FNDI.