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References

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  2. Semsarian, JI, Ingles, J, Maron, MS, et.al. New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy. J Am Coll Cardiol. 2015; 65: 1249-64. https://doi.org/10.1016/j.jacc.2015.01.019.

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  4. Maron BJ, Rowin EJ, Casey SA, et al. How hypertrophic cardiomyopathy became a contemporary treatable genetic disease with low mortality: shaped by 50 years of clinical research and practice. JAMA Cardiol. 2016;1:98–105. doi:10.1001/jamacardio.2015.0354

  5. Maron, BJ, Maron, MS, Rowin, EG. Perspectives on the overall risks of living with hypertrophic cardiomyopathy. Circulation. 2017;135:2317–2319. https://doi.org/10.1161/CIRCULATIONAHA.117.027738

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  8. Ingles, J, Burns, C, Bagnall, RD, et.al. Nonfamiliar Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications. Circ Cardiovasc Genet. 2017;10:e001620. https://doi.org/10.1161/CIRCGENETICS.116.001620

  9. Ho, CY, Day, SM, Ashley, EA, et.al. Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe). Circulation. 2018;138:1387–1398. DOI: 10.1161/CIRCULATIONAHA.117.033200

  10. MyoKardia, Inc., a wholly owned subsidiary of Bristol Myers Squibb. CAMZYOSTM (mavacamten): US prescribing information. 2022. https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214998s000lbl.pdf.

  11. Spertus, JA, Fine, JT, Elliott, P, et.al. Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): health status analysis of a randomized, double-blind, placebo-controlled, phase 3 trial. Lancet. 2022 May 21; 397(10293):2467-2475. https://doi.org/10.1016/S0140-6736(21)00763-7.

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  13. Nguyen A, Schaff HV. Surgical Myectomy: Subaortic, Midventricular, and Apical. Cardiol Clin. 2019 Feb;37(1):95-104. PMID: 3044772014.

  14. Shah AA, Glower DD, Gaca JG. Trans-aortic Alfieri stitch at the time of septal myectomy for hypertrophic obstructive cardiomypopathy. J Card Surg. 2016;31:503-506. PMID: 27401021

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