Vallespin, E <br/><br/>
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hd0510.  [electronic resource] 

 -  Human genetics  Feb 2006 
 - 774 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Eye Proteins--genetics<br/>Gene Deletion<br/>Humans<br/>Membrane Proteins--genetics<br/>Nerve Tissue Proteins--genetics<br/>Optic Atrophy, Hereditary, Leber--genetics