Zeitz, Christina <br/><br/>
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.  [electronic resource] 

 -  American journal of human genetics  Jan 2013 
 - 67-75 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.2012.10.023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Exome<br/>Eye Diseases, Hereditary--genetics<br/>Female<br/>Genetic Diseases, X-Linked--genetics<br/>Humans<br/>Male<br/>Membrane Proteins--analysis<br/>Middle Aged<br/>Mutation<br/>Myopia--genetics<br/>Night Blindness--genetics<br/>Polymorphism, Genetic<br/>Retina--chemistry