New Variant of <i>MYH7</i> Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course-Reference-Cited by-同舟云学术

New Variant of MYH7 Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course

Published:2020-07-04 Issue:3 Volume:16 Page:383-391
ISSN:2225-3653
Container-title:Rational Pharmacotherapy in Cardiology
language:
Short-container-title:Racionalʹnaâ farmakoterapiâ v kardiologii

Author:

Myasnikov R. P.¹,Kulikova O. V.¹,Meshkov A. N.¹,Kiseleva A. V.¹,Shumarina A. O.¹,Koretskiy S. N.¹,Zharikova A. A.¹,Divashuk M. G.²,Kharlap M. S.¹,Serduk S. E.¹,Mershina E. A.³,Sinitsyn V. E.³,Boytsov S. A.⁴,Drapkina O. M.¹

Affiliation:

1. National Medical Research Center for Therapy and Preventive Medicine

2. National Medical Research Center for Therapy and Preventive Medicine; Kurchatov Genomics Center, All-Russia Research Institute of Agricultural Biotechnology

3. Lomonosov Moscow State University

4. National Medical Research Center of Cardiology

Publisher

Stolichnaya Izdatelskaya Kompaniyaizdat

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

Reference23 articles.

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2. Caliskan K., Michels M., Geleijnse M.L., et al. Frequency of Asymptomatic Disease Among Family Members With Non-compaction Cardiomyopathy. The American Journal of Cardiology. 2012;110(10):1512-7. DOI:10.1016/j.amjcard.2012.07.009.

3. Myasnikov R.P., Shcherbakova N.V., Kulikova O.V. i dr. Mutatsiya gena DES v sem'e probanda s miofibrillyarnoi miopatiei i razvitiem nekompaktnoi kardiomiopatii, privedshei k transplantatsii serdtsa. Rossiiskii Kardiologicheskii Zhurnal. 2017;10(150):9-16. DOI:10.15829/1560-4071-2017-10-9-16.

4. Finsterer J., Stollberger C. Primary prophylactic anticoagulation is mandatory if non-compaction is associated with atrial fibrillation or heart failure. International Journal of Cardiology. 2015;184(1):268-69. DOI:10.1016/j.ijcard.2015.02.041.

5. Jacquier A., Thuny F., Jop B., et al. Measurement of trabeculated left ventricular mass using cardiac magnetic resonance imaging in the diagnosis of left ventricular non-compaction. Eur Heart J. 2010;31(9):1098-104. DOI:10.1093/eurheartj/ehp595.

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1. Genetic landscape in Russian patients with familial left ventricular noncompaction;Frontiers in Cardiovascular Medicine;2023-05-24

2. A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy;Genes;2022-09-28

3. The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report;International Journal of Molecular Sciences;2021-06-24

4. New variant of PRDM16 gene nucleotide sequence in a family with various phenotypic manifestations of the non-compacted myocardium;Russian Journal of Cardiology;2021-04-22