Vallespin, E <br/><br/>
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0534.  [electronic resource] 

 -  Human genetics  Feb 2006 
 - 777 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Eye Proteins--genetics<br/>Humans<br/>Membrane Proteins--genetics<br/>Mutation, Missense<br/>Nerve Tissue Proteins--genetics<br/>Optic Atrophy, Hereditary, Leber--genetics