Audo, Isabelle <br/><br/>
TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.  [electronic resource] 

 -  American journal of human genetics  Nov 2009 
 - 720-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2009.10.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Electroretinography<br/>Female<br/>Genes, Recessive<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Male<br/>Models, Genetic<br/>Mutation<br/>Night Blindness--congenital<br/>Nuclear Family<br/>Pedigree<br/>TRPM Cation Channels--genetics