Perrault, Isabelle <br/><br/>
Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis.  [electronic resource] 

 -  American journal of human genetics  Oct 2004 
 - 639-46 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/424889  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alcohol Oxidoreductases--genetics<br/>Amino Acid Sequence<br/>Base Sequence<br/>Blindness--congenital<br/>Chromatography, Liquid<br/>DNA Mutational Analysis<br/>DNA Primers<br/>Humans<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Optic Atrophy, Hereditary, Leber--genetics<br/>Pedigree<br/>Sequence Alignment