<i>CASQ2</i>: clinical and genetic insights into catecholaminergic polymorphic ventricular tachycardia across three families
Catecholaminergic polymorphic ventricular tachycardia is a primary channelopathy with a high mortality rate if left untreated. In 3 to 5% of catecholaminergic polymorphic ventricular tachycardia patients, mutations in the CASQ2 gene, either in a homozygous or compound heterozygous form, have been id...
| Main Authors: | , |
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| Format: | Article |
| Language: | Russian |
| Published: |
MONIKI
2023-08-01
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| Series: | Alʹmanah Kliničeskoj Mediciny |
| Subjects: | |
| Online Access: | https://almclinmed.ru/jour/article/viewFile/7699/1583 |