Baig, Shahid M <br/><br/>
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness.  [electronic resource] 

 -  Nature neuroscience  Jan 2011 
 - 77-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1726 
<br/><br/><label>Standard No.: </label>10.1038/nn.2694  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Bradycardia--genetics<br/>Calcium Channels, L-Type--genetics<br/>Channelopathies--genetics<br/>Deafness--congenital<br/>Female<br/>HEK293 Cells<br/>Hair Cells, Auditory, Inner--physiology<br/>Haplotypes<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Protein Isoforms--genetics<br/>Sinoatrial Node--physiology<br/>Syndrome<br/>Transfection--methods