Ma, J <br/><br/>
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.  [electronic resource] 

 -  Genomics  Jul 1995 
 - 212-9 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>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.1995.1133  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>DNA Transposable Elements<br/>DNA, Complementary--genetics<br/>Exons--genetics<br/>Eye Proteins--genetics<br/>Gene Library<br/>Genes<br/>Haplotypes--genetics<br/>Intermediate Filament Proteins--genetics<br/>Membrane Glycoproteins<br/>Mice<br/>Mice, Inbred BALB C<br/>Mice, Neurologic Mutants--genetics<br/>Molecular Sequence Data<br/>Mutagenesis, Insertional<br/>Nerve Tissue Proteins<br/>Peripherins<br/>Retinal Degeneration--genetics