Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness. [electronic resource]
Producer: 20110203Description: 77-84 p. digitalISSN:- 1546-1726
- Adolescent
- Adult
- Bradycardia -- genetics
- Calcium Channels, L-Type -- genetics
- Channelopathies -- genetics
- Deafness -- congenital
- Female
- HEK293 Cells
- Hair Cells, Auditory, Inner -- physiology
- Haplotypes
- Humans
- Male
- Mutation
- Pedigree
- Protein Isoforms -- genetics
- Sinoatrial Node -- physiology
- Syndrome
- Transfection -- methods
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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