Nichols, B E <br/><br/>
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.  [electronic resource] 

 -  Human molecular genetics  May 1993 
 - 601-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/2.5.601  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Base Sequence<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Eye Proteins--genetics<br/>Female<br/>Fovea Centralis<br/>Humans<br/>Intermediate Filament Proteins<br/>Macular Degeneration--genetics<br/>Male<br/>Membrane Glycoproteins<br/>Molecular Sequence Data<br/>Nerve Tissue Proteins<br/>Pedigree<br/>Peripherins<br/>Sequence Deletion