Mice Lacking <i>Gpr179</i> with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia
Mutations in <i>GPR179</i> are one of the most common causes of autosomal recessive complete congenital stationary night blindness (cCSNB). This retinal disease is characterized in patients by impaired dim and night vision, associated with other ocular symptoms, including high myopia. cC...
Main Authors: | Baptiste Wilmet, Jacques Callebert, Robert Duvoisin, Ruben Goulet, Christophe Tourain, Christelle Michiels, Helen Frederiksen, Frank Schaeffel, Olivier Marre, José Alain Sahel, Isabelle Audo, Serge Picaud, Christina Zeitz |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-12-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/24/1/219 |
Similar Items
-
A New Mouse Model for Complete Congenital Stationary Night Blindness Due to <i>Gpr179</i> Deficiency
by: Elise Orhan, et al.
Published: (2021-04-01) -
Characterization of Four Orphan Receptors (GPR3, GPR6, GPR12 and GPR12L) in Chickens and Ducks and Regulation of <i>GPR12</i> Expression in Ovarian Granulosa Cells by Progesterone
by: Zejiao Li, et al.
Published: (2021-03-01) -
Mutation in the RPE65 gene causing hereditary retinal dystrophy in the Briard dogs: application of a new detection method
by: R. Bechyňová, et al.
Published: (2008-04-01) -
Determination of Lactose Concentration in Milk Serum by Refractometry and Polarimetry
by: Rodica Caprita, et al.
Published: (2023-09-01) -
Suppression of Air Refractive Index Variations in High-Resolution Interferometry
by: Zdeněk Buchta, et al.
Published: (2011-08-01)