Zhang, K <br/><br/>
A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.  [electronic resource] 

 -  American journal of ophthalmology  Dec 1999 
 - 720-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9394 
<br/><br/><label>Standard No.: </label>10.1016/s0002-9394(99)00236-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--genetics<br/>Adult<br/>Base Sequence<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Eye Diseases, Hereditary--genetics<br/>Female<br/>Fluorescein Angiography<br/>Fundus Oculi<br/>Humans<br/>Macular Degeneration--genetics<br/>Middle Aged<br/>Molecular Sequence Data<br/>Pedigree<br/>Point Mutation<br/>Polymorphism, Single-Stranded Conformational<br/>Sequence Analysis, DNA<br/>Visual Acuity