Familial central diabetes insipidus
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Utility of genetic testing in suspected familial cranial diabetes insipidus;Srinivasan;Endocrinol Diabetes Metab Case Rep,2013
2. AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus;Turkkahraman;Pituitary,2015
3. Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus – benefit of genetic testing;Hrčková;Eur J Pediatr,2016
4. Magnetic resonance in familial central diabetes insipidus: a family study;Bastida Eizaguirre;An Esp Pediatr,1996
5. Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation;McLeod;J Clin Endocrinol Metab,1993
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