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

Abstract

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. METHODS Four patients with neurohypophyseal diabetes insipidus… (More)
DOI: 10.1007/s40618-015-0357-9

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