Klevering, B J <br/><br/>
Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene.  [electronic resource] 

 -  The British journal of ophthalmology  Aug 1999 
 - 914-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1161 
<br/><br/><label>Standard No.: </label>10.1136/bjo.83.8.914  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--genetics<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Consanguinity<br/>Female<br/>Genotype<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Night Blindness--genetics<br/>Pedigree<br/>Phenotype<br/>Retinal Degeneration--genetics<br/>Visual Acuity--genetics<br/>Visual Fields--genetics