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Seminars in Nephrology
Volume 26, Issue 3
, Pages 209-223
, May 2006
Familial Neurohypophyseal Diabetes Insipidus—An Update
References
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- A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus . Mol Genet Metab . 1999;67:89–92
- A new mutation of the arginine vasopressin-neurophysin II gene in a family with autosomal dominant neurohypophyseal diabetes insipidus . Exp Clin Endocrinol Diabetes . 2001;109:406–409
- A missense mutation encoding cys(67) –> gly in neurophysin II is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus . Mol Genet Metab . 2001;72:39–44
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Supported in part by the Institute of Clinical Medicine, Aarhus University; the Karen Elise Jensen Foundation; and the Novo Nordisk Foundation.
PII: S0270-9295(06)00030-1
doi: 10.1016/j.semnephrol.2006.03.003
© 2006 Elsevier Inc. All rights reserved.
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Seminars in Nephrology
Volume 26, Issue 3
, Pages 209-223
, May 2006
