Naylor, M J <br/><br/>
Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness.  [electronic resource] 

 -  Genomics  Jun 2000 
 - 324-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.2000.6204  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Calcium Channels--genetics<br/>Calcium Channels, L-Type--genetics<br/>DNA Primers<br/>Eye--metabolism<br/>Humans<br/>In Situ Hybridization<br/>Mice<br/>Molecular Sequence Data<br/>Night Blindness--genetics<br/>Organ Specificity<br/>Physical Chromosome Mapping<br/>RNA, Messenger--biosynthesis<br/>Retina--metabolism<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Sequence Analysis, DNA<br/>Sequence Homology, Nucleic Acid<br/>X Chromosome--genetics