Spectrum of mutations and their phenotypic manifestations in children and adults with long QT syndrome
Aim. To determine the spectrum of mutations in the genes responsible for the long QT syndrome (LQTS) and study their phenotypic manifestations in patients with LQTS in different age groups.Materials and methods. The study included 35 unrelated probands with a clinical diagnosis of LQTS: 23 adults (8...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | Russian |
Published: |
«FIRMA «SILICEA» LLC
2021-11-01
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Series: | Российский кардиологический журнал |
Subjects: | |
Online Access: | https://russjcardiol.elpub.ru/jour/article/view/4704 |