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Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family

Autosomal dominant neurohypophyseal diabetes insipidus is a rare form of central diabetes insipidus that is caused by mutations in the vasopressin-neurophysin II (AVP-NPII) gene. It is characterized by persistent polydipsia and polyuria induced by deficient or absent secretion of arginine vasopressi...

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Detalles Bibliográficos
Autores principales:	Kim, Myo-Jing, Kim, Young-Eun, Ki, Chang-Seok, Yoo, Jae-Ho
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Society of Pediatric Endocrinology 2014
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4316416/ https://www.ncbi.nlm.nih.gov/pubmed/25654069 http://dx.doi.org/10.6065/apem.2014.19.4.220

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