MUTATION SPECTRUM OF THE GENE KCNQ1 IN RUSSIAN PATIENTS WITH LONG QT SYNDROME
The primary long QT syndrome (LQTS) is hereditary disorder of cardiac rhythm. More than 15 genetic types of the disease known. Most prevalent is the type of the disorder related to potassium channel KvLQT1.Aim. Analysis of mutation spectrum in the gene KCNQ1, coding α-subunit of potassium channel IK...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
«FIRMA «SILICEA» LLC
2016-10-01
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| Series: | Российский кардиологический журнал |
| Subjects: | |
| Online Access: | https://russjcardiol.elpub.ru/jour/article/view/951 |