Riazuddin, S Amer <br/><br/>
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.  [electronic resource] 

 -  American journal of human genetics  Oct 2010 
 - 523-31 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.2010.08.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Chromosomes, Human, Pair 15--genetics<br/>Genes, Recessive<br/>Humans<br/>Immunohistochemistry<br/>In Situ Hybridization<br/>Mice<br/>Molecular Sequence Data<br/>Night Blindness--genetics<br/>Retina--metabolism<br/>Sequence Analysis, DNA<br/>Sequence Deletion--genetics<br/>Sodium-Calcium Exchanger--genetics