Analysis of mutations spectrum in the KCNQ1, KCNH2 and SCN5A genes in patients with long QT syndrome using massively parallel sequencing

A. A. Sivtsev; L. I. Svintsova; I. V. Plotnikova; I. Zh. Zhalsanova; A. E. Postrigan; L. I. Minaicheva; O. Yu. Dzhaffarova; N. A. Skryabin

Medical Genetics
Medicinskaâ genetika

ISSN 2073-7998 (Print)

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Sivtsev A.A., Svintsova L.I., Plotnikova I.V., Zhalsanova I.Zh., Postrigan A.E., Minaicheva L.I., Dzhaffarova O.Yu., Skryabin N.A. Analysis of mutations spectrum in the KCNQ1, KCNH2 and SCN5A genes in patients with long QT syndrome using massively parallel sequencing. Medical Genetics. 2020;19(5):20-22. (In Russ.) https://doi.org/10.25557/2073-7998.2020.05.20-22

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ISSN 2073-7998 (Print)

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About the Authors

A. A. Sivtsev
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

L. I. Svintsova
Cardiology Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

I. V. Plotnikova
Cardiology Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

I. Zh. Zhalsanova
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

A. E. Postrigan
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

L. I. Minaicheva
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

O. Yu. Dzhaffarova
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

N. A. Skryabin
Research Institute of Medical Genetics, Tomsk National Research Medical Center of the Russian Academy of Sciences
Russian Federation

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