Publication: A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus
Loading...
Program
relationships.isAuthorOf
Author
Ilhan, MAHMUT MUZAFFER
KARAMAN, O.
YILDIZ, R. S.
TURGUT, SEDA
TOPRAK, HÜSEYİN
Advisor
Date
Language
Type
Publisher
Journal Title
Journal ISSN
Volume Title
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.
Description
Source
Keywords
Keywords
Citation
Ilhan M. M. , Tiryakioglu N. O. , KARAMAN O., Coskunpinar E., YILDIZ R. S. , TURGUT S., Tiryakioglu D., TOPRAK H., TASAN E., -A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus-, JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, cilt.39, ss.285-290, 2016