A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus

Ilhan, MAHMUT MUZAFFERTiryakioglu, N. O.KARAMAN, O.Coskunpinar, E.YILDIZ, R. S.TURGUT, SEDATiryakioglu, D.TOPRAK, HÜSEYİNTASAN, ERTUĞRUL2019-10-052019-10-052016-03-01Ilhan M. M. , Tiryakioglu N. O. , KARAMAN O., Coskunpinar E., YILDIZ R. S. , TURGUT S., Tiryakioglu D., TOPRAK H., TASAN E., -A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus-, JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, cilt.39, ss.285-290, 2016https://hdl.handle.net/20.500.12645/3149Purpose 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.enA novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidusArticleWOS:0003708426000058495905083210.1007/s40618-015-0357-926208472