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...
Main Authors: | Myo-Jing Kim, Young-Eun Kim, Chang-Seok Ki, Jae-Ho Yoo |
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Format: | Article |
Language: | English |
Published: |
Korean Society of Pediatric Endocrinology
2014-12-01
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Series: | Annals of Pediatric Endocrinology & Metabolism |
Subjects: | |
Online Access: | http://e-apem.org/upload/pdf/apem-19-220.pdf |
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