Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System
- 7 February 2003
- journal article
- case report
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 92 (2) , 159-168
- https://doi.org/10.1161/01.res.0000052672.97759.36
Abstract
Cardiac conduction defects associate with mutations in SCN5A, the gene encoding the cardiac Na+ channel. In the present study, we characterized a family in which the proband was born in severe dist...Keywords
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