Peachey, Neal S <br/><br/>
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.  [electronic resource] 

 -  American journal of human genetics  Feb 2012 
 - 331-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2011.12.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Chromosome Mapping--methods<br/>Dark Adaptation--genetics<br/>Electroretinography--methods<br/>Eye Diseases, Hereditary<br/>Gene Knockdown Techniques--methods<br/>Genetic Diseases, X-Linked<br/>Heterozygote<br/>Humans<br/>Mice<br/>Mice, Inbred C3H<br/>Mice, Inbred C57BL<br/>Mutation<br/>Myopia--genetics<br/>Night Blindness--genetics<br/>Pedigree<br/>Receptors, G-Protein-Coupled--genetics<br/>Receptors, Metabotropic Glutamate--genetics<br/>Retinal Bipolar Cells--metabolism<br/>Retinal Rod Photoreceptor Cells--metabolism<br/>Signal Transduction<br/>Zebrafish