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Tropomyosin–troponin complex in inherited cardiomyopathies
Krijger, C., Sequeira, V., van den Boogaard, M., Veerman, C. C., Hoetjes, N. J., Poel, E., Tanck, M. W. T., Lekanne Deprez, R. H., Vermeer, A. M. C., van der Velden, J., Amin, A. S. & Juárez, C. K., Jul 2024, In: Heart Rhythm. 21, 7, p. 1173-1175 3 p.Research output: Contribution to journal › Article › Academic › peer-review
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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
de Brouwer, R., Hassanzada, F., Schoemaker, A. E., Schmidt, A. F., Kooijman-Reumerman, M. D., Bracun, V., Slieker, M. G., Dooijes, D., Vermeer, A. M. C., Wilde, A. A. M., Amin, A. S., Lekanne Deprez, R. H., Herkert, J. C., Christiaans, I., de Boer, R. A., Jongbloed, J. D. H., van Tintelen, J. P. & Baas, A. F., Jan 2024, In: JACC: Heart Failure. 12, 1, p. 134-147 14 p.Research output: Contribution to journal › Article › Academic › peer-review
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MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset
The European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart, 1 Aug 2023, In: Netherlands heart journal. 31, 7-8, p. 300-307 8 p.Research output: Contribution to journal › Article › Academic › peer-review
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