Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathy
Author:
Funder
Korea National Institute of Health
Korea Disease Control and Prevention Agency
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1186/s12920-024-02000-8.pdf
Reference54 articles.
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2. de Frutos F, Ochoa JP, Navarro-Penalver M, Baas A, Bjerre JV, Zorio E, et al. Natural history of MYH7-Related dilated cardiomyopathy. J Am Coll Cardiol. 2022;80(15):1447–61.
3. Velicki L, Jakovljevic DG, Preveden A, Golubovic M, Bjelobrk M, Ilic A, et al. Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy. BMC Cardiovasc Disord. 2020;20(1):516.
4. McNally EM, Golbus JR, Puckelwartz MJ. Genetic mutations and mechanisms in dilated cardiomyopathy. J Clin Invest. 2013;123(1):19–26.
5. Olivotto I, Girolami F, Ackerman MJ, Nistri S, Bos JM, Zachara E, et al. Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy. Mayo Clin Proc. 2008;83(6):630–8.
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