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Long qt syndrome : Genetic analysis of patients. / Dementyeva, E. V.; Medvedev, S. P.; Elisaphenko, E. A. et al.

In: Genes and Cells, Vol. 13, No. 4, 01.01.2018, p. 75-80.

Research output: Contribution to journal › Article › peer-review

Harvard

Dementyeva, EV, Medvedev, SP, Elisaphenko, EA, Bayramova, SA, Pokushalov, EA, Agladze, KI & Zakian, SM 2018, 'Long qt syndrome: Genetic analysis of patients', Genes and Cells, vol. 13, no. 4, pp. 75-80. https://doi.org/10.23868/201812050

APA

Dementyeva, E. V., Medvedev, S. P., Elisaphenko, E. A., Bayramova, S. A., Pokushalov, E. A., Agladze, K. I., & Zakian, S. M. (2018). Long qt syndrome: Genetic analysis of patients. Genes and Cells, 13(4), 75-80. https://doi.org/10.23868/201812050

Vancouver

Dementyeva EV, Medvedev SP, Elisaphenko EA, Bayramova SA, Pokushalov EA, Agladze KI et al. Long qt syndrome: Genetic analysis of patients. Genes and Cells. 2018 Jan 1;13(4):75-80. doi: 10.23868/201812050

Author

Dementyeva, E. V. ; Medvedev, S. P. ; Elisaphenko, E. A. et al. / Long qt syndrome : Genetic analysis of patients. In: Genes and Cells. 2018 ; Vol. 13, No. 4. pp. 75-80.

BibTeX

@article{9f4d08cc8f3e46d582837ca497cd92f1,
title = "Long qt syndrome: Genetic analysis of patients",
abstract = "Genetic analysis plays an important role in diagnostics of cardiovascular diseases. One of the diseases is long QT syndrome that results in an increased risk of ventricular tachycardia and sudden cardiac death. The syndrome may be caused by mutations in genes responsible for cardiomyocyte ionic channel functioning. The aim of this study is to examine genetics of long QT syndrome. Genetic analysis of 16 patients with long QT syndrome or suspicion of the syndrome was carried out. Long QT syndrome causing mutations, p.Ala178Pro, p.Val254Met, p.Gly325Arg in KCNQ1 and p.Thr613Met in KCNH2, and a long QT syndrome-associated polymorphism, p.Asp85Asn in KCNE1, were found in five patients. Family analysis of p.Ala178Pro and p.Val254Met mutations in KCNQ1 revealed the mutations carriers that had not demonstrated any syndrome manifestations before. In addition, a mutation, p.Gly604Ala in KCNH2, was found. The mutation has not been previously described and its role in long QT syndrome needs to be clarified.",
keywords = "Long QT syndrome, Mutation, Syncope, Ventricular tachycardia",
author = "Dementyeva, {E. V.} and Medvedev, {S. P.} and Elisaphenko, {E. A.} and Bayramova, {S. A.} and Pokushalov, {E. A.} and Agladze, {K. I.} and Zakian, {S. M.}",
year = "2018",
month = jan,
day = "1",
doi = "10.23868/201812050",
language = "English",
volume = "13",
pages = "75--80",
journal = "Genes and Cells",
issn = "2313-1829",
publisher = "Human Stem Cells Institute OJSC (HSCI)",
number = "4",

}

RIS

TY - JOUR

T1 - Long qt syndrome

T2 - Genetic analysis of patients

AU - Dementyeva, E. V.

AU - Medvedev, S. P.

AU - Elisaphenko, E. A.

AU - Bayramova, S. A.

AU - Pokushalov, E. A.

AU - Agladze, K. I.

AU - Zakian, S. M.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Genetic analysis plays an important role in diagnostics of cardiovascular diseases. One of the diseases is long QT syndrome that results in an increased risk of ventricular tachycardia and sudden cardiac death. The syndrome may be caused by mutations in genes responsible for cardiomyocyte ionic channel functioning. The aim of this study is to examine genetics of long QT syndrome. Genetic analysis of 16 patients with long QT syndrome or suspicion of the syndrome was carried out. Long QT syndrome causing mutations, p.Ala178Pro, p.Val254Met, p.Gly325Arg in KCNQ1 and p.Thr613Met in KCNH2, and a long QT syndrome-associated polymorphism, p.Asp85Asn in KCNE1, were found in five patients. Family analysis of p.Ala178Pro and p.Val254Met mutations in KCNQ1 revealed the mutations carriers that had not demonstrated any syndrome manifestations before. In addition, a mutation, p.Gly604Ala in KCNH2, was found. The mutation has not been previously described and its role in long QT syndrome needs to be clarified.

AB - Genetic analysis plays an important role in diagnostics of cardiovascular diseases. One of the diseases is long QT syndrome that results in an increased risk of ventricular tachycardia and sudden cardiac death. The syndrome may be caused by mutations in genes responsible for cardiomyocyte ionic channel functioning. The aim of this study is to examine genetics of long QT syndrome. Genetic analysis of 16 patients with long QT syndrome or suspicion of the syndrome was carried out. Long QT syndrome causing mutations, p.Ala178Pro, p.Val254Met, p.Gly325Arg in KCNQ1 and p.Thr613Met in KCNH2, and a long QT syndrome-associated polymorphism, p.Asp85Asn in KCNE1, were found in five patients. Family analysis of p.Ala178Pro and p.Val254Met mutations in KCNQ1 revealed the mutations carriers that had not demonstrated any syndrome manifestations before. In addition, a mutation, p.Gly604Ala in KCNH2, was found. The mutation has not been previously described and its role in long QT syndrome needs to be clarified.

KW - Long QT syndrome

KW - Mutation

KW - Syncope

KW - Ventricular tachycardia

UR - http://www.scopus.com/inward/record.url?scp=85064632675&partnerID=8YFLogxK

U2 - 10.23868/201812050

DO - 10.23868/201812050

M3 - Article

AN - SCOPUS:85064632675

VL - 13

SP - 75

EP - 80

JO - Genes and Cells

JF - Genes and Cells

SN - 2313-1829

IS - 4

ER -

ID: 19647832