Perrault, Isabelle <br/><br/>
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype.  [electronic resource] 

 -  PloS one  2013 
 - e51622 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0051622  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Canada<br/>Child<br/>Child, Preschool<br/>China<br/>Cohort Studies<br/>Europe<br/>Eye Proteins--genetics<br/>Female<br/>Humans<br/>Infant<br/>Leber Congenital Amaurosis--genetics<br/>Linkage Disequilibrium<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Genetic<br/>Retina--metabolism<br/>Retinal Degeneration--genetics<br/>United States<br/>Young Adult