Amsterdam Cardiovascular Sciences
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Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes (Genetics in Medicine, (2019), 21, 2, (319-330), 10.1038/s41436-018-0048-y): Aminoacyl-tRNA synthetase deficiencies in search of common themes
Fuchs, S. A., Schene, I. F., Kok, G., Jansen, J. M., Nikkels, P. G. J., van Gassen, K. L. I., Terheggen-Lagro, S. W. J., van der Crabben, S. N., Hoeks, S. E., Niers, L. E. M., Wolf, N. I., de Vries, M. C., Koolen, D. A., Houwen, R. H. J., Mulder, M. F. & van Hasselt, P. M., Oct 2021, In: Genetics in medicine. 23, 10, p. 2024Research output: Contribution to journal › Article* › Academic › peer-review
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Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case: A heterozygous and a homozygous case
Bruyndonckx, L., Vogelzang, J. L., Bugiani, M., Straver, B., Kuipers, I. M., Onland, W., Nannenberg, E. A., Clur, S.-A. & & van der Crabben, S. N., Aug 2021, In: American journal of medical genetics. Part A. 185, 8, p. 2464-2470 7 p.Research output: Contribution to journal › Article* › Academic › peer-review
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BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status
Jansen, M., Christiaans, I., van der Crabben, S. N., Michels, M., Huurman, R., Hoedemaekers, Y. M., Dooijes, D., Jongbloed, J. D. H., Boven, L. G., Lekanne Deprez, R. H., Wilde, A. A. M., Jans, J. J. M., van der Velden, J., de Boer, R. A., van Tintelen, J. P., Asselbergs, F. W. & Baas, A. F., Jun 2021, In: Netherlands heart journal. 29, 6, p. 318-329 12 p.Research output: Contribution to journal › Article* › Academic › peer-review
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