Novel compound aquaporin 2 mutations in nephrogenic diabetes insipidus
Main Authors: | Raphael D Liberatore Junior, Juliana G Carneiro, Franciele B Leidenz, Rachel Melilo-Carolino, Helena C Sarubi, Luiz De Marco |
---|---|
Format: | Article |
Language: | English |
Published: |
Faculdade de Medicina / USP
2012-01-01
|
Series: | Clinics |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322012000100013 |
Similar Items
-
Molecular Characterization of an Aquaporin−2 Mutation Causing Nephrogenic Diabetes Insipidus
by: Qian Li, et al.
Published: (2021-08-01) -
A Case of Congenital Nephrogenic Diabetes Insipidus Caused by Thr108Met Variant of Aquaporin 2
by: Lina Ma, et al.
Published: (2020-01-01) -
New insights into the transcriptional regulation of aquaporin-2 and the treatment of X-linked hereditary nephrogenic diabetes insipidus
by: Hyun Jun Jung, et al.
Published: (2019-06-01) -
Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patients
by: Maria Helena Vaisbich, et al.
Published: (2009-05-01) -
Molecular Genetic Study of Nephrogenic Diabetes Insipidus
by: Wen-Yu Chen, et al.
Published: (1999)