Publication details
Clinical, genetic and biophysical characterization of three novel SCN5A mutations in patients with Brugada syndrome
| Authors | |
|---|---|
| Year of publication | 2006 |
| Type | Conference abstract |
| MU Faculty or unit | |
| Citation | |
| Description | Three new SCN5A mutations were detected in patients with Brugada syndrome, two of them frameshift mutations with complete loss of function and one missense mutation with decreased function and impaired inactivation gating. |
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